'dysplasie acromicrique'
(id=1832489 ; fe=dysplasie acromicrique ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=11083 creation date=2015-07-30 touchdate=2025-12-24 13:47:52.000) ≈ 521 relations sortantes
- dysplasie acromicrique --
r_associated #0: 42 / 1 ->
en:keratitis, hereditary
n1=dysplasie acromicrique | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=42
- dysplasie acromicrique --
r_associated #0: 41 / 0.976 ->
en:autosomal dominant charcot-marie-tooth disease type 2a1
n1=dysplasie acromicrique | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=41
- dysplasie acromicrique --
r_associated #0: 41 / 0.976 ->
en:hnsha due to triosephosphate isomerase deficiency
n1=dysplasie acromicrique | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=41
- dysplasie acromicrique --
r_associated #0: 41 / 0.976 ->
en:morquio syndrome
n1=dysplasie acromicrique | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=41
- dysplasie acromicrique --
r_associated #0: 41 / 0.976 ->
en:multicentric osteolysis nodulosis arthropathy spectrum
n1=dysplasie acromicrique | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=41
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough
n1=dysplasie acromicrique | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps
n1=dysplasie acromicrique | n2=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:becker generalized myotonia
n1=dysplasie acromicrique | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:congenital absence of foot
n1=dysplasie acromicrique | n2=en:congenital absence of foot | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:congenital subluxation of carpus
n1=dysplasie acromicrique | n2=en:congenital subluxation of carpus | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:dolichocephalic dwarfism
n1=dysplasie acromicrique | n2=en:dolichocephalic dwarfism | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:dyssegmental dysplasia with glaucoma syndrome
n1=dysplasie acromicrique | n2=en:dyssegmental dysplasia with glaucoma syndrome | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:familial hemiplegic migraine
n1=dysplasie acromicrique | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:familial isolated arrhythmogenic right ventricular dysplasia
n1=dysplasie acromicrique | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:hereditary motor and sensory neuropathy type i
n1=dysplasie acromicrique | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:marfan syndrome
n1=dysplasie acromicrique | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:melanoma astrocytoma syndrome
n1=dysplasie acromicrique | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:nicolaides baraitser syndrome
n1=dysplasie acromicrique | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:pseudocholinesterase deficiency
n1=dysplasie acromicrique | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:spinocerebellar ataxia 29
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:stickler syndrome
n1=dysplasie acromicrique | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:transverse deficiency of hand
n1=dysplasie acromicrique | n2=en:transverse deficiency of hand | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
en:triglyceride storage disease with ichthyosis
n1=dysplasie acromicrique | n2=en:triglyceride storage disease with ichthyosis | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 40 / 0.952 ->
syndrome de Moore-Federman
n1=dysplasie acromicrique | n2=syndrome de Moore-Federman | rel=r_associated | relid=0 | w=40
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:acute intermittent porphyria
n1=dysplasie acromicrique | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:auriculo-condylar syndrome
n1=dysplasie acromicrique | n2=en:auriculo-condylar syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:autosomal dominant analbuminemia
n1=dysplasie acromicrique | n2=en:autosomal dominant analbuminemia | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:autosomal dominant deficiency of plasminogen
n1=dysplasie acromicrique | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:autosomal dominant excess of transthyretin
n1=dysplasie acromicrique | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:autosomal dominant hypophosphatemic bone disease
n1=dysplasie acromicrique | n2=en:autosomal dominant hypophosphatemic bone disease | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:autosomal dominant mutilating keratoderma
n1=dysplasie acromicrique | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:blau syndrome
n1=dysplasie acromicrique | n2=en:blau syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:brachydactyly of toes
n1=dysplasie acromicrique | n2=en:brachydactyly of toes | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:brody myopathy
n1=dysplasie acromicrique | n2=en:brody myopathy | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:cataract, congenital, cerulean type 1
n1=dysplasie acromicrique | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:cone-shaped epiphysis
n1=dysplasie acromicrique | n2=en:cone-shaped epiphysis | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:congenital nephrogenic diabetes insipidus
n1=dysplasie acromicrique | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:cutis laxa, autosomal dominant
n1=dysplasie acromicrique | n2=en:cutis laxa, autosomal dominant | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:donohue syndrome
n1=dysplasie acromicrique | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:dyskeratosis congenita, autosomal dominant
n1=dysplasie acromicrique | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:ectrodactyly
n1=dysplasie acromicrique | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:fleck corneal dystrophy
n1=dysplasie acromicrique | n2=en:fleck corneal dystrophy | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:haspeslagh fryns muelenaere syndrome
n1=dysplasie acromicrique | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:hereditary elliptocytosis due to alpha spectrin defect
n1=dysplasie acromicrique | n2=en:hereditary elliptocytosis due to alpha spectrin defect | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:hereditary papillary renal cell carcinoma
n1=dysplasie acromicrique | n2=en:hereditary papillary renal cell carcinoma | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:hyaline dystrophy of bruch's membrane
n1=dysplasie acromicrique | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:hyperinsulinemic hypoglycemia, familial, 6
n1=dysplasie acromicrique | n2=en:hyperinsulinemic hypoglycemia, familial, 6 | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1
n1=dysplasie acromicrique | n2=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies
n1=dysplasie acromicrique | n2=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:klippel-trenaunay-weber syndrome
n1=dysplasie acromicrique | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:kuskokwim disease
n1=dysplasie acromicrique | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:may-hegglin anomaly
n1=dysplasie acromicrique | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:microcornea with glaucoma and absent frontal sinus syndrome
n1=dysplasie acromicrique | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:mullerian duct and limb anomalies syndrome
n1=dysplasie acromicrique | n2=en:mullerian duct and limb anomalies syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:muscle amp deaminase deficiency
n1=dysplasie acromicrique | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:potassium aggravated myotonia
n1=dysplasie acromicrique | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:prune belly syndrome
n1=dysplasie acromicrique | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:roch leri mesosomatous lipomatosis
n1=dysplasie acromicrique | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:schnyder crystalline corneal dystrophy
n1=dysplasie acromicrique | n2=en:schnyder crystalline corneal dystrophy | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:shwachman-diamond syndrome
n1=dysplasie acromicrique | n2=en:shwachman-diamond syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 39 / 0.929 ->
en:wellesley carman french syndrome
n1=dysplasie acromicrique | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=39
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:acrodysostosis
n1=dysplasie acromicrique | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth
n1=dysplasie acromicrique | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:asexual dwarfism
n1=dysplasie acromicrique | n2=en:asexual dwarfism | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:autosomal dominant hyperinsulinism due to kir6.2 deficiency
n1=dysplasie acromicrique | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:autosomal dominant idiopathic familial dystonia
n1=dysplasie acromicrique | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:autosomal dominant pterygium of conjunctiva
n1=dysplasie acromicrique | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:autosomal dominant variant form of albumin
n1=dysplasie acromicrique | n2=en:autosomal dominant variant form of albumin | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:bilateral pheochromocytoma and islet cell adenoma of the pancreas
n1=dysplasie acromicrique | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055)
n1=dysplasie acromicrique | n2=en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055) | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:chondrodysplasia punctata syndrome
n1=dysplasie acromicrique | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:choreoathetosis/spasticity, episodic
n1=dysplasie acromicrique | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:chromosome 22q11.2 microduplication syndrome
n1=dysplasie acromicrique | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:cole disease
n1=dysplasie acromicrique | n2=en:cole disease | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:congenital absence of hand
n1=dysplasie acromicrique | n2=en:congenital absence of hand | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:congenital hand agenesis
n1=dysplasie acromicrique | n2=en:congenital hand agenesis | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:congenital hereditary muscular dystrophy
n1=dysplasie acromicrique | n2=en:congenital hereditary muscular dystrophy | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:congenital short quadriceps
n1=dysplasie acromicrique | n2=en:congenital short quadriceps | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:cranioectodermal dysplasia
n1=dysplasie acromicrique | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:crouzon syndrome with acanthosis nigricans (disorder)
n1=dysplasie acromicrique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:deep philtrum
n1=dysplasie acromicrique | n2=en:deep philtrum | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:familial arthrogryposis-cholestatic hepatorenal syndrome
n1=dysplasie acromicrique | n2=en:familial arthrogryposis-cholestatic hepatorenal syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:familial spontaneous pneumothorax
n1=dysplasie acromicrique | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:fbn1, tyr1699cys
n1=dysplasie acromicrique | n2=en:fbn1, tyr1699cys | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:freeman-sheldon syndrome
n1=dysplasie acromicrique | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:gaze palsy, familial horizontal, with progressive scoliosis
n1=dysplasie acromicrique | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:generalized myotonia of thomsen
n1=dysplasie acromicrique | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:glycogen storage disease, muscular form
n1=dysplasie acromicrique | n2=en:glycogen storage disease, muscular form | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:hereditary systemic amyloidosis
n1=dysplasie acromicrique | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:laron syndrome
n1=dysplasie acromicrique | n2=en:laron syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:marden-walker syndrome
n1=dysplasie acromicrique | n2=en:marden-walker syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:metatropic dwarfism
n1=dysplasie acromicrique | n2=en:metatropic dwarfism | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:mild facial anomalies
n1=dysplasie acromicrique | n2=en:mild facial anomalies | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis
n1=dysplasie acromicrique | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:neurofibromatosis type 2
n1=dysplasie acromicrique | n2=en:neurofibromatosis type 2 | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:neuropathy, hereditary motor and sensory, okinawa type
n1=dysplasie acromicrique | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:peripheral resistance to thyroid hormone
n1=dysplasie acromicrique | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:pituitary adenoma, familial isolated (disorder)
n1=dysplasie acromicrique | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:prader-willi habitus, osteopenia, and camptodactyly
n1=dysplasie acromicrique | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:primary hypertrophic osteoarthropathy
n1=dysplasie acromicrique | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:radial aplasia-thrombocytopenia syndrome
n1=dysplasie acromicrique | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:sellars beighton syndrome
n1=dysplasie acromicrique | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:spinocerebellar ataxia 28
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:synpolydactyly
n1=dysplasie acromicrique | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:thanatophoric dysplasia
n1=dysplasie acromicrique | n2=en:thanatophoric dysplasia | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:thick skin
n1=dysplasie acromicrique | n2=en:thick skin | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:transthyretin related familial amyloid cardiomyopathy
n1=dysplasie acromicrique | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:treacher collins syndrome
n1=dysplasie acromicrique | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 38 / 0.905 ->
en:tylosis
n1=dysplasie acromicrique | n2=en:tylosis | rel=r_associated | relid=0 | w=38
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:alpha-fetoprotein, hereditary persistence of
n1=dysplasie acromicrique | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:andersen syndrome
n1=dysplasie acromicrique | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:aplasia of lacrimal and salivary glands
n1=dysplasie acromicrique | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:autosomal dominant charcot-marie-tooth disease type 2c
n1=dysplasie acromicrique | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:autosomal dominant cystoid macular edema
n1=dysplasie acromicrique | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:brachydactyly, type a1 (disorder)
n1=dysplasie acromicrique | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:capillary malformation-arteriovenous malformation (disorder)
n1=dysplasie acromicrique | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:charcot-marie-tooth disease, axonal, type 2l (disorder)
n1=dysplasie acromicrique | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:congenital anomaly of toe
n1=dysplasie acromicrique | n2=en:congenital anomaly of toe | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:congenital bowing of long bone
n1=dysplasie acromicrique | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:congenital spade-like hand
n1=dysplasie acromicrique | n2=en:congenital spade-like hand | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:congenital talipes varus
n1=dysplasie acromicrique | n2=en:congenital talipes varus | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:diastrophic dysplasia
n1=dysplasie acromicrique | n2=en:diastrophic dysplasia | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:distal arthrogryposis syndrome
n1=dysplasie acromicrique | n2=en:distal arthrogryposis syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:dopa-responsive dystonia
n1=dysplasie acromicrique | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:duplication of the whole foot
n1=dysplasie acromicrique | n2=en:duplication of the whole foot | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:ectodermal dysplasia/ skin fragility syndrome
n1=dysplasie acromicrique | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:familial hypercalciuric hypocalcemia
n1=dysplasie acromicrique | n2=en:familial hypercalciuric hypocalcemia | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:fibrodysplasia ossificans progressiva
n1=dysplasie acromicrique | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:gurrieri sammito bellussi syndrome
n1=dysplasie acromicrique | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:hereditary cerebral amyloid angiopathy, icelandic type
n1=dysplasie acromicrique | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:insulin autoimmune syndrome
n1=dysplasie acromicrique | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:knobloch syndrome
n1=dysplasie acromicrique | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:laurin-sandrow syndrome
n1=dysplasie acromicrique | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:long philtrum
n1=dysplasie acromicrique | n2=en:long philtrum | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:longitudinal deficiency of tibia and/or fibula
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of tibia and/or fibula | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
n1=dysplasie acromicrique | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:neurofibromatosis type 1
n1=dysplasie acromicrique | n2=en:neurofibromatosis type 1 | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:papillon-lefevre syndrome
n1=dysplasie acromicrique | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:reardon hall slaney syndrome
n1=dysplasie acromicrique | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:reticulate acropigmentation of kitamura
n1=dysplasie acromicrique | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:rud syndrome
n1=dysplasie acromicrique | n2=en:rud syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:short palms
n1=dysplasie acromicrique | n2=en:short palms | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:spondylo-ocular syndrome
n1=dysplasie acromicrique | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:type ii acrocephalopolysyndactyly
n1=dysplasie acromicrique | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 37 / 0.881 ->
en:verloes bourguignon syndrome
n1=dysplasie acromicrique | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=37
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:aberrant intrinsic muscles of hand
n1=dysplasie acromicrique | n2=en:aberrant intrinsic muscles of hand | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:antley-bixler syndrome, autosomal dominant
n1=dysplasie acromicrique | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:autosomal dominant muscular dystrophy not predominantly limb girdle
n1=dysplasie acromicrique | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:bannayan syndrome
n1=dysplasie acromicrique | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:centronuclear myopathy 1
n1=dysplasie acromicrique | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:cleidocranial dysplasia
n1=dysplasie acromicrique | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:congenital anomaly of finger
n1=dysplasie acromicrique | n2=en:congenital anomaly of finger | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:congenital malformation of thumb
n1=dysplasie acromicrique | n2=en:congenital malformation of thumb | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:corneal dystrophy, congenital stromal
n1=dysplasie acromicrique | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:duplication of whole hand
n1=dysplasie acromicrique | n2=en:duplication of whole hand | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:epiphyseal dysplasia, multiple, 1
n1=dysplasie acromicrique | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:hereditary angioedema
n1=dysplasie acromicrique | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:hypothyroid dwarfism
n1=dysplasie acromicrique | n2=en:hypothyroid dwarfism | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:jackson-weiss syndrome
n1=dysplasie acromicrique | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:jeune syndrome
n1=dysplasie acromicrique | n2=en:jeune syndrome | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:keratosis palmoplantaris papulosa
n1=dysplasie acromicrique | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:longitudinal deficiency of radius
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of radius | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:lynch syndrome
n1=dysplasie acromicrique | n2=en:lynch syndrome | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:metaphyseal dysplasia, braun-tinschert type
n1=dysplasie acromicrique | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:myopathy with exercise intolerance, swedish type
n1=dysplasie acromicrique | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:nonaka myopathy
n1=dysplasie acromicrique | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:otoonychoperoneal syndrome
n1=dysplasie acromicrique | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:piebaldism
n1=dysplasie acromicrique | n2=en:piebaldism | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:plantarflexed cuboid
n1=dysplasie acromicrique | n2=en:plantarflexed cuboid | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:short, stubby metacarpals
n1=dysplasie acromicrique | n2=en:short, stubby metacarpals | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:shprintzen omphalocele syndrome
n1=dysplasie acromicrique | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:spinocerebellar ataxia 1s
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia 1s | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:spinocerebellar ataxia 36
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:split foot
n1=dysplasie acromicrique | n2=en:split foot | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:steinfeld syndrome
n1=dysplasie acromicrique | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:tmem70 related mitochondrial encephalo-cardio-myopathy
n1=dysplasie acromicrique | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:vitreoretinochoroidopathy (disorder)
n1=dysplasie acromicrique | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 36 / 0.857 ->
en:wnt4 mullerian aplasia and ovarian dysfunction
n1=dysplasie acromicrique | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=36
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:beare-stevenson cutis gyrata syndrome
n1=dysplasie acromicrique | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:brachydactyly type a6
n1=dysplasie acromicrique | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:chondrodysplasia, grebe type
n1=dysplasie acromicrique | n2=en:chondrodysplasia, grebe type | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:congenital deformity of right hand
n1=dysplasie acromicrique | n2=en:congenital deformity of right hand | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:congenital malformation syndromes associated with short stature
n1=dysplasie acromicrique | n2=en:congenital malformation syndromes associated with short stature | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:congenital short achilles tendon
n1=dysplasie acromicrique | n2=en:congenital short achilles tendon | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:cystinosis, infantile nephropathic
n1=dysplasie acromicrique | n2=en:cystinosis, infantile nephropathic | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:dwarfism
n1=dysplasie acromicrique | n2=en:dwarfism | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:fifth metacarpal with ulnar notch
n1=dysplasie acromicrique | n2=en:fifth metacarpal with ulnar notch | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:glucose transporter protein type 1 deficiency syndrome
n1=dysplasie acromicrique | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:glycogen storage disease type x
n1=dysplasie acromicrique | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:hereditary diffuse gastric adenocarcinoma
n1=dysplasie acromicrique | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:hereditary tubulointerstitial disorder
n1=dysplasie acromicrique | n2=en:hereditary tubulointerstitial disorder | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:lethal congenital contracture syndrome 2
n1=dysplasie acromicrique | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:multiple endocrine neoplasia type 2b
n1=dysplasie acromicrique | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:neuropathy, hereditary thermosensitive
n1=dysplasie acromicrique | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:pitt-hopkins syndrome
n1=dysplasie acromicrique | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:potocki-shaffer syndrome
n1=dysplasie acromicrique | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:robinow syndrome
n1=dysplasie acromicrique | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:saito kuba tsuruta syndrome
n1=dysplasie acromicrique | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:second metacarpal notched proximally on radial side
n1=dysplasie acromicrique | n2=en:second metacarpal notched proximally on radial side | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:spinocerebellar ataxia type 7
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:thiel-behnke corneal dystrophy
n1=dysplasie acromicrique | n2=en:thiel-behnke corneal dystrophy | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:tryptophanuria with dwarfism
n1=dysplasie acromicrique | n2=en:tryptophanuria with dwarfism | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 35 / 0.833 ->
en:ulna metaphyseal dysplasia syndrome
n1=dysplasie acromicrique | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=35
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
dysplasie géléophysique
n1=dysplasie acromicrique | n2=dysplasie géléophysique | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
n1=dysplasie acromicrique | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:alagille syndrome
n1=dysplasie acromicrique | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:arthrogryposis, distal, type 1
n1=dysplasie acromicrique | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:autosomal dominant epidermolysis bullosa simplex
n1=dysplasie acromicrique | n2=en:autosomal dominant epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:autosomal dominant ichthyosis vulgaris
n1=dysplasie acromicrique | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:autosomal dominant oculocutaneous albinism
n1=dysplasie acromicrique | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:autosomal dominant optic atrophy
n1=dysplasie acromicrique | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:avascular necrosis of femoral head
n1=dysplasie acromicrique | n2=en:avascular necrosis of femoral head | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:bilateral multiple fibroadenoma of breast
n1=dysplasie acromicrique | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:brachydactyly of hand
n1=dysplasie acromicrique | n2=en:brachydactyly of hand | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:brachydactyly syndrome type c
n1=dysplasie acromicrique | n2=en:brachydactyly syndrome type c | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:brachydactyly syndrome type e
n1=dysplasie acromicrique | n2=en:brachydactyly syndrome type e | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:brachyolmia type 3
n1=dysplasie acromicrique | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:brooke-spiegler syndrome
n1=dysplasie acromicrique | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:charcot-marie-tooth disease, axonal, type 2b (disorder)
n1=dysplasie acromicrique | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:charcot-marie-tooth disease, type 2j
n1=dysplasie acromicrique | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:chromosome 17q21.31 deletion syndrome
n1=dysplasie acromicrique | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:congenital anomaly of metacarpal bone
n1=dysplasie acromicrique | n2=en:congenital anomaly of metacarpal bone | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:congenital anomaly of tarsal bone
n1=dysplasie acromicrique | n2=en:congenital anomaly of tarsal bone | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:congenital dyserythropoietic anemia, type iii
n1=dysplasie acromicrique | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:congenital finger deformity
n1=dysplasie acromicrique | n2=en:congenital finger deformity | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:congenital foot deformity
n1=dysplasie acromicrique | n2=en:congenital foot deformity | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:congenital valgus deformity of foot
n1=dysplasie acromicrique | n2=en:congenital valgus deformity of foot | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:cutis laxa, autosomal recessive
n1=dysplasie acromicrique | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:de sanctis-cacchione syndrome
n1=dysplasie acromicrique | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:dentatorubral-pallidoluysian atrophy
n1=dysplasie acromicrique | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:ectodermal dysplasia with natal teeth, turnpenny type
n1=dysplasie acromicrique | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:familial encephalopathy with neuroserpin inclusion bodies
n1=dysplasie acromicrique | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:familial hypodontia
n1=dysplasie acromicrique | n2=en:familial hypodontia | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:familial interstitial nephritis
n1=dysplasie acromicrique | n2=en:familial interstitial nephritis | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:fbn1, tyr1700cys
n1=dysplasie acromicrique | n2=en:fbn1, tyr1700cys | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:feingold syndrome
n1=dysplasie acromicrique | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:femur bifid with monodactylous ectrodactyly
n1=dysplasie acromicrique | n2=en:femur bifid with monodactylous ectrodactyly | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:fibular hypoplasia and complex brachydactyly
n1=dysplasie acromicrique | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:frontotemporal dementia
n1=dysplasie acromicrique | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:glomuvenous malformations
n1=dysplasie acromicrique | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:hereditary benign intraepithelial dyskeratosis
n1=dysplasie acromicrique | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:hereditary elliptocytosis due to beta spectrin defect in self-association
n1=dysplasie acromicrique | n2=en:hereditary elliptocytosis due to beta spectrin defect in self-association | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:hereditary elliptocytosis due to deficiency of protein 4.1
n1=dysplasie acromicrique | n2=en:hereditary elliptocytosis due to deficiency of protein 4.1 | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:hereditary multiple exostoses
n1=dysplasie acromicrique | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:hereditary stomatocytosis
n1=dysplasie acromicrique | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:hyperferritinemia, hereditary, with congenital cataracts
n1=dysplasie acromicrique | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:hypophosphatemic rickets with hypercalciuria, hereditary
n1=dysplasie acromicrique | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:idiopathic short stature
n1=dysplasie acromicrique | n2=en:idiopathic short stature | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:inherited arthrogryposis
n1=dysplasie acromicrique | n2=en:inherited arthrogryposis | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:leopard syndrome
n1=dysplasie acromicrique | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:lethal congenital contracture syndrome 1
n1=dysplasie acromicrique | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:lethal congenital contracture syndrome type 3
n1=dysplasie acromicrique | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:lissencephaly syndrome, norman-roberts type
n1=dysplasie acromicrique | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:loeys-dietz syndrome
n1=dysplasie acromicrique | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:menkes disease
n1=dysplasie acromicrique | n2=en:menkes disease | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:mesomelic dwarfism reinhardt pfeiffer type
n1=dysplasie acromicrique | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:muscle l-lactate dehydrogenase deficiency
n1=dysplasie acromicrique | n2=en:muscle l-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:myopathy with abnormal lipid metabolism
n1=dysplasie acromicrique | n2=en:myopathy with abnormal lipid metabolism | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:myopathy, distal 2
n1=dysplasie acromicrique | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:nathalie syndrome
n1=dysplasie acromicrique | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:non-dystrophic myotonia
n1=dysplasie acromicrique | n2=en:non-dystrophic myotonia | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:noonan syndrome
n1=dysplasie acromicrique | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:oculodental syndrome rutherfurd syndrome
n1=dysplasie acromicrique | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:ovoid vertebral bodies
n1=dysplasie acromicrique | n2=en:ovoid vertebral bodies | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:paroxysmal extreme pain disorder
n1=dysplasie acromicrique | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:pituitary dwarfism
n1=dysplasie acromicrique | n2=en:pituitary dwarfism | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:polydactyly, preaxial ii (disorder)
n1=dysplasie acromicrique | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:reis-bucklers' corneal dystrophy
n1=dysplasie acromicrique | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:smith-mccort dysplasia
n1=dysplasie acromicrique | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:spondyloperipheral dysplasia short ulna
n1=dysplasie acromicrique | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:sting-associated vasculopathy with onset in infancy
n1=dysplasie acromicrique | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:strudwick syndrome
n1=dysplasie acromicrique | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:syndactyly, type i
n1=dysplasie acromicrique | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:syndactyly, type iii
n1=dysplasie acromicrique | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:syndrome, branchio-oculo-facial
n1=dysplasie acromicrique | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:type v acrocephalosyndactyly
n1=dysplasie acromicrique | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 34 / 0.81 ->
en:von willebrand disease, platelet type
n1=dysplasie acromicrique | n2=en:von willebrand disease, platelet type | rel=r_associated | relid=0 | w=34
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:abnormal palmar creases
n1=dysplasie acromicrique | n2=en:abnormal palmar creases | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:abnormal plantar creases
n1=dysplasie acromicrique | n2=en:abnormal plantar creases | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:achondrogenesis
n1=dysplasie acromicrique | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:advanced sleep-phase syndrome, familial
n1=dysplasie acromicrique | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:albright's hereditary osteodystrophy
n1=dysplasie acromicrique | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:arthrogryposis multiplex congenita, neurogenic type (disorder)
n1=dysplasie acromicrique | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:autosomal dominant late onset basal ganglia degeneration
n1=dysplasie acromicrique | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:autosomal dominant polycystic kidney disease
n1=dysplasie acromicrique | n2=en:autosomal dominant polycystic kidney disease | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:baller-gerold syndrome
n1=dysplasie acromicrique | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:benign autosomal dominant osteopetrosis
n1=dysplasie acromicrique | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:benign congenital myopathy
n1=dysplasie acromicrique | n2=en:benign congenital myopathy | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:brachyphalangia of toe
n1=dysplasie acromicrique | n2=en:brachyphalangia of toe | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:bulbous nose
n1=dysplasie acromicrique | n2=en:bulbous nose | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:char syndrome
n1=dysplasie acromicrique | n2=en:char syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:chronic infantile neurological cutaneous and articular syndrome
n1=dysplasie acromicrique | n2=en:chronic infantile neurological cutaneous and articular syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:col1a1 associated connective tissue disorder
n1=dysplasie acromicrique | n2=en:col1a1 associated connective tissue disorder | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:congenital
n1=dysplasie acromicrique | n2=en:congenital | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:congenital claw foot
n1=dysplasie acromicrique | n2=en:congenital claw foot | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:congenital overgrowth of foot
n1=dysplasie acromicrique | n2=en:congenital overgrowth of foot | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:congenital shortening of upper arm
n1=dysplasie acromicrique | n2=en:congenital shortening of upper arm | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:craniofacial deafness hand syndrome
n1=dysplasie acromicrique | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:delayed bone age
n1=dysplasie acromicrique | n2=en:delayed bone age | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:dominant autosomal hereditary disorder, complete penetrance
n1=dysplasie acromicrique | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:dystrophia myotonica 2
n1=dysplasie acromicrique | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:ehlers-danlos syndrome
n1=dysplasie acromicrique | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:epidermolysis bullosa simplex with pyloric atresia
n1=dysplasie acromicrique | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:epilepsy, myoclonic, benign adult familial, type 2
n1=dysplasie acromicrique | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:episodic ataxia
n1=dysplasie acromicrique | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:epithelial recurrent erosion dystrophy
n1=dysplasie acromicrique | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:fronto-facio-nasal dysplasia
n1=dysplasie acromicrique | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:frontotemporal dementia, chromosome 3-linked
n1=dysplasie acromicrique | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:generalized epilepsy and paroxysmal dyskinesia syndrome
n1=dysplasie acromicrique | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:geniospasm 1
n1=dysplasie acromicrique | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:giacci familial neurogenic acroosteolysis
n1=dysplasie acromicrique | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:growth cartilage disorganized, with islands of cells and abnormal collagen arrangement
n1=dysplasie acromicrique | n2=en:growth cartilage disorganized, with islands of cells and abnormal collagen arrangement | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hand deformities
n1=dysplasie acromicrique | n2=en:hand deformities | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hand foot uterus syndrome
n1=dysplasie acromicrique | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hereditary cystatin c amyloid angiopathy
n1=dysplasie acromicrique | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hereditary mucosal leukokeratosis
n1=dysplasie acromicrique | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hereditary nonpolyposis colorectal cancer
n1=dysplasie acromicrique | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:heritable pulmonary arterial hypertension due to bmpr2 mutation
n1=dysplasie acromicrique | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hoarseness
n1=dysplasie acromicrique | n2=en:hoarseness | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hyperinsulinism due to hnf4a deficiency
n1=dysplasie acromicrique | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hyperpigmentation, familial progressive
n1=dysplasie acromicrique | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:hypoplastic tibia and postaxial polydactyly syndrome
n1=dysplasie acromicrique | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:iris coloboma with ptosis, hypertelorism, and mental retardation
n1=dysplasie acromicrique | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:kbg syndrome
n1=dysplasie acromicrique | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:klippel-feil syndrome
n1=dysplasie acromicrique | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:li-fraumeni syndrome
n1=dysplasie acromicrique | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:long eyelashes
n1=dysplasie acromicrique | n2=en:long eyelashes | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:miller-mckusick-malvaux-syndrome (3m syndrome)
n1=dysplasie acromicrique | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:mowat-wilson syndrome
n1=dysplasie acromicrique | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:nemaline myopathy 3
n1=dysplasie acromicrique | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:o/e - short stature
n1=dysplasie acromicrique | n2=en:o/e - short stature | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:parietal foramina
n1=dysplasie acromicrique | n2=en:parietal foramina | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:popliteal pterygium syndrome
n1=dysplasie acromicrique | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:proteus-like syndrome (disorder)
n1=dysplasie acromicrique | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:pseudohypoaldosteronism, type 1, dominant form
n1=dysplasie acromicrique | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:rachitic dwarf
n1=dysplasie acromicrique | n2=en:rachitic dwarf | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:short long bone
n1=dysplasie acromicrique | n2=en:short long bone | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:short stature associated with bone marrow transplant
n1=dysplasie acromicrique | n2=en:short stature associated with bone marrow transplant | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:spinocerebellar ataxia type 2
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:spinocerebellar ataxia type 5
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:spinocerebellar ataxia type 6 (disorder)
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:spondyloenchondrodysplasia
n1=dysplasie acromicrique | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:symbrachydactyly of toe
n1=dysplasie acromicrique | n2=en:symbrachydactyly of toe | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:undergrowth of whole hand
n1=dysplasie acromicrique | n2=en:undergrowth of whole hand | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:vitelliform macular dystrophy
n1=dysplasie acromicrique | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 33 / 0.786 ->
en:well-defined eyebrows
n1=dysplasie acromicrique | n2=en:well-defined eyebrows | rel=r_associated | relid=0 | w=33
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:amelogenesis imperfecta, type ib
n1=dysplasie acromicrique | n2=en:amelogenesis imperfecta, type ib | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:atelosteogenesis, type 1
n1=dysplasie acromicrique | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autoimmune lymphoproliferative syndrome
n1=dysplasie acromicrique | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autosomal dominant hyperinsulinism due to sur1 deficiency
n1=dysplasie acromicrique | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
n1=dysplasie acromicrique | n2=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autosomal dominant ichthyosis
n1=dysplasie acromicrique | n2=en:autosomal dominant ichthyosis | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autosomal dominant inheritance
n1=dysplasie acromicrique | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autosomal dominant retinitis pigmentosa
n1=dysplasie acromicrique | n2=en:autosomal dominant retinitis pigmentosa | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autosomal recessive distal osteolysis syndrome
n1=dysplasie acromicrique | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:autosomal recessive muscular dystrophy with limb girdle distribution
n1=dysplasie acromicrique | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:birth length less than 3rd percentile
n1=dysplasie acromicrique | n2=en:birth length less than 3rd percentile | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:brachymetatarsia
n1=dysplasie acromicrique | n2=en:brachymetatarsia | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:cerebral hemorrhage with amyloidosis, hereditary, dutch type
n1=dysplasie acromicrique | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:cochleosaccular degeneration of the inner ear and progressive cataracts
n1=dysplasie acromicrique | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:congenital anomaly of metatarsal bone
n1=dysplasie acromicrique | n2=en:congenital anomaly of metatarsal bone | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:currarino triad
n1=dysplasie acromicrique | n2=en:currarino triad | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:dicer1 syndrome
n1=dysplasie acromicrique | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:dominant beta-thalassemia
n1=dysplasie acromicrique | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:dwarfism, alopecia, pseudoanodontia, cutis laxa
n1=dysplasie acromicrique | n2=en:dwarfism, alopecia, pseudoanodontia, cutis laxa | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:dysostosis multiplex group
n1=dysplasie acromicrique | n2=en:dysostosis multiplex group | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:familial creutzfeldt-jakob
n1=dysplasie acromicrique | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:familial partial lipodystrophy, type 2
n1=dysplasie acromicrique | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:fbn1, ser1750arg
n1=dysplasie acromicrique | n2=en:fbn1, ser1750arg | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related
n1=dysplasie acromicrique | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:genitopatellar syndrome
n1=dysplasie acromicrique | n2=en:genitopatellar syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:hereditary sensory autonomic neuropathy, type 1
n1=dysplasie acromicrique | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:hyperinsulinemic hypoglycemia, familial, 7
n1=dysplasie acromicrique | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:infantile dwarf
n1=dysplasie acromicrique | n2=en:infantile dwarf | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:insulin growth factor i resistance
n1=dysplasie acromicrique | n2=en:insulin growth factor i resistance | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:internal notch of femoral head
n1=dysplasie acromicrique | n2=en:internal notch of femoral head | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:lamellar ichthyosis, autosomal dominant form
n1=dysplasie acromicrique | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:longitudinal deficiency of femur
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of femur | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:longitudinal deficiency of humerus
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of humerus | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:longitudinal deficiency of left fibula
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of left fibula | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome
n1=dysplasie acromicrique | n2=en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:macdermot winter syndrome
n1=dysplasie acromicrique | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:macrodactyly of the hand
n1=dysplasie acromicrique | n2=en:macrodactyly of the hand | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:macular corneal dystrophy
n1=dysplasie acromicrique | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:majeed syndrome
n1=dysplasie acromicrique | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:microphthalmia, syndromic 3
n1=dysplasie acromicrique | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:nail-patella syndrome
n1=dysplasie acromicrique | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:nevoid basal cell carcinoma syndrome
n1=dysplasie acromicrique | n2=en:nevoid basal cell carcinoma syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:osteogenesis imperfecta, levin type
n1=dysplasie acromicrique | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:pyle metaphyseal dysplasia
n1=dysplasie acromicrique | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:rhizomelic chondrodysplasia punctata
n1=dysplasie acromicrique | n2=en:rhizomelic chondrodysplasia punctata | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:round face
n1=dysplasie acromicrique | n2=en:round face | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:short stature co-occurrent and due to endocrine disorder
n1=dysplasie acromicrique | n2=en:short stature co-occurrent and due to endocrine disorder | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:short stature due to radiation therapy
n1=dysplasie acromicrique | n2=en:short stature due to radiation therapy | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:short stature with valvular heart disease and characteristic facies syndrome
n1=dysplasie acromicrique | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:spinocerebellar ataxia 8
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:spinocerebellar ataxia type 4
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:spondylocostal dysostosis 4, autosomal dominant
n1=dysplasie acromicrique | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:spondyloepiphyseal dysplasia tarda, x-linked
n1=dysplasie acromicrique | n2=en:spondyloepiphyseal dysplasia tarda, x-linked | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:spondyloepiphyseal dysplasia, omani type
n1=dysplasie acromicrique | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:steatocystoma multiplex
n1=dysplasie acromicrique | n2=en:steatocystoma multiplex | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:type i acrocephalosyndactyly
n1=dysplasie acromicrique | n2=en:type i acrocephalosyndactyly | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:ulnar-mammary syndrome
n1=dysplasie acromicrique | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:whyte hemingway carpal tarsal phalangeal osteolyses
n1=dysplasie acromicrique | n2=en:whyte hemingway carpal tarsal phalangeal osteolyses | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 32 / 0.762 ->
en:zimmerman laband syndrome
n1=dysplasie acromicrique | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=32
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
dysplasie
n1=dysplasie acromicrique | n2=dysplasie | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:abnormally short growth
n1=dysplasie acromicrique | n2=en:abnormally short growth | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:adult onset autosomal dominant leukodystrophy
n1=dysplasie acromicrique | n2=en:adult onset autosomal dominant leukodystrophy | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:ameloonychohypohidrotic syndrome
n1=dysplasie acromicrique | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:anteverted nostril
n1=dysplasie acromicrique | n2=en:anteverted nostril | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:autosomal dominant progressive nephropathy with hypertension
n1=dysplasie acromicrique | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:behavioral variant of frontotemporal dementia
n1=dysplasie acromicrique | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:bone development disorder
n1=dysplasie acromicrique | n2=en:bone development disorder | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:charcot-marie-tooth disease type 2d
n1=dysplasie acromicrique | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:chromosome 3q29 deletion syndrome
n1=dysplasie acromicrique | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:congenital dysplasia
n1=dysplasie acromicrique | n2=en:congenital dysplasia | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:congenital reticular ichthyosiform erythroderma
n1=dysplasie acromicrique | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:craniodiaphyseal dysplasia
n1=dysplasie acromicrique | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:deformity of digit of hand due to amniotic band
n1=dysplasie acromicrique | n2=en:deformity of digit of hand due to amniotic band | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:diplopodia
n1=dysplasie acromicrique | n2=en:diplopodia | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:dominant autosomal hereditary disorder, incomplete penetrance
n1=dysplasie acromicrique | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
n1=dysplasie acromicrique | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:familial amyloid polyneuropathy, type v
n1=dysplasie acromicrique | n2=en:familial amyloid polyneuropathy, type v | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:familial benign neonatal epilepsy
n1=dysplasie acromicrique | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:familial non-autoimmune autosomal dominant hyperthyroidism
n1=dysplasie acromicrique | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:familial osteochondritis dissecans
n1=dysplasie acromicrique | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:fbn1, ala1728thr
n1=dysplasie acromicrique | n2=en:fbn1, ala1728thr | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:geleophysic dysplasia
n1=dysplasie acromicrique | n2=en:geleophysic dysplasia | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:glycogen storage disease 0, liver
n1=dysplasie acromicrique | n2=en:glycogen storage disease 0, liver | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:goniodysgenesis-mental retardation-short stature syndrome
n1=dysplasie acromicrique | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:hereditary gastrogenic lactose intolerance
n1=dysplasie acromicrique | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:hereditary oculoleptomeningeal amyloid angiopathy
n1=dysplasie acromicrique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:holoprosencephaly with fetal akinesia-hypokinesia sequence
n1=dysplasie acromicrique | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:hypotrichosis simplex of scalp
n1=dysplasie acromicrique | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:liddle syndrome
n1=dysplasie acromicrique | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:limb deformities, congenital
n1=dysplasie acromicrique | n2=en:limb deformities, congenital | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:longitudinal deficiency of left femur
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of left femur | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:longitudinal deficiency of metacarpal bone
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of metacarpal bone | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:longitudinal deficiency of phalanges of hand
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of phalanges of hand | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:longitudinal deficiency of ulna
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of ulna | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:microcephaly deafness syndrome
n1=dysplasie acromicrique | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:muckle-wells syndrome
n1=dysplasie acromicrique | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:neurofibromatosis, type 1-like syndrome
n1=dysplasie acromicrique | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:nutritional stunting
n1=dysplasie acromicrique | n2=en:nutritional stunting | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:okihiro syndrome
n1=dysplasie acromicrique | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:peutz-jeghers syndrome
n1=dysplasie acromicrique | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:polyostotic fibrous dysplasia
n1=dysplasie acromicrique | n2=en:polyostotic fibrous dysplasia | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:proportionate short stature
n1=dysplasie acromicrique | n2=en:proportionate short stature | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:pseudomuscular build
n1=dysplasie acromicrique | n2=en:pseudomuscular build | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:renal dwarfism
n1=dysplasie acromicrique | n2=en:renal dwarfism | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:sebastian syndrome
n1=dysplasie acromicrique | n2=en:sebastian syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:senile dwarfism
n1=dysplasie acromicrique | n2=en:senile dwarfism | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:short foot
n1=dysplasie acromicrique | n2=en:short foot | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:short, stubby phalanges
n1=dysplasie acromicrique | n2=en:short, stubby phalanges | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:spinocerebellar ataxia 10
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:split-hand-foot malformation with long bone deficiency 1
n1=dysplasie acromicrique | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:spondyloenchondrodysplasia with immune dysregulation
n1=dysplasie acromicrique | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:spondyloepiphyseal dysplasia tarda, toledo type
n1=dysplasie acromicrique | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:tarsal coalitions
n1=dysplasie acromicrique | n2=en:tarsal coalitions | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:tarsal-carpal coalition syndrome
n1=dysplasie acromicrique | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:wells jankovic syndrome
n1=dysplasie acromicrique | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 31 / 0.738 ->
en:windblown hand
n1=dysplasie acromicrique | n2=en:windblown hand | rel=r_associated | relid=0 | w=31
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:brachydactyly syndrome type b
n1=dysplasie acromicrique | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:cerebral cavernous malformation
n1=dysplasie acromicrique | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:hereditary myopathy with early respiratory failure
n1=dysplasie acromicrique | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:hypermobility syndrome
n1=dysplasie acromicrique | n2=en:hypermobility syndrome | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:longitudinal deficiency of carpal bone
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of carpal bone | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:mandibuloacral dysplasia with type a lipodystrophy
n1=dysplasie acromicrique | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:microcephaly cervical spine fusion anomalies
n1=dysplasie acromicrique | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:pulmonary interstitial glycogenosis
n1=dysplasie acromicrique | n2=en:pulmonary interstitial glycogenosis | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:syndromic orbital border hypoplasia
n1=dysplasie acromicrique | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 30 / 0.714 ->
en:ulnar dimelia
n1=dysplasie acromicrique | n2=en:ulnar dimelia | rel=r_associated | relid=0 | w=30
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:brachymesophalangy 2 and 5
n1=dysplasie acromicrique | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:cap myopathy
n1=dysplasie acromicrique | n2=en:cap myopathy | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:farber lipogranulomatosis
n1=dysplasie acromicrique | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:geroderma osteodysplastica
n1=dysplasie acromicrique | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:hawkinsinuria
n1=dysplasie acromicrique | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:heide syndrome
n1=dysplasie acromicrique | n2=en:heide syndrome | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:hunter-thompson dysplasia
n1=dysplasie acromicrique | n2=en:hunter-thompson dysplasia | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:hyperinsulinism due to deficiency of glucokinase
n1=dysplasie acromicrique | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:myopathy, distal, tateyama type
n1=dysplasie acromicrique | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 29 / 0.69 ->
en:radial hypoplasia, triphalangeal thumbs and hypospadias
n1=dysplasie acromicrique | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=29
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:dysplasia, saddan
n1=dysplasie acromicrique | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:familial amyloid neuropathy
n1=dysplasie acromicrique | n2=en:familial amyloid neuropathy | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:familial digital arthropathy and brachydactyly syndrome
n1=dysplasie acromicrique | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:fbn1, 3-bp dup, nt5202
n1=dysplasie acromicrique | n2=en:fbn1, 3-bp dup, nt5202 | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:foxg1 syndrome
n1=dysplasie acromicrique | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:hereditary breast and ovarian cancer syndrome
n1=dysplasie acromicrique | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia
n1=dysplasie acromicrique | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:mauriac's syndrome
n1=dysplasie acromicrique | n2=en:mauriac's syndrome | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:myhre syndrome
n1=dysplasie acromicrique | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
n1=dysplasie acromicrique | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 28 / 0.667 ->
en:spinocerebellar ataxia 31 (disorder)
n1=dysplasie acromicrique | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=28
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:autosomal dominant familial woolly hair
n1=dysplasie acromicrique | n2=en:autosomal dominant familial woolly hair | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:deafness-craniofacial syndrome
n1=dysplasie acromicrique | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:ehlers-danlos syndrome, type i
n1=dysplasie acromicrique | n2=en:ehlers-danlos syndrome, type i | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:hereditary elliptocytosis due to abnormal protein 4.1
n1=dysplasie acromicrique | n2=en:hereditary elliptocytosis due to abnormal protein 4.1 | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:melnick-fraser syndrome
n1=dysplasie acromicrique | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:multiple epiphyseal dysplasia type 5
n1=dysplasie acromicrique | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:pseudohypoparathyroidism and pseudopseudohypoparathyroidism type i
n1=dysplasie acromicrique | n2=en:pseudohypoparathyroidism and pseudopseudohypoparathyroidism type i | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 27 / 0.643 ->
en:thick vermilion border
n1=dysplasie acromicrique | n2=en:thick vermilion border | rel=r_associated | relid=0 | w=27
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:acromicric dysplasia
n1=dysplasie acromicrique | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:asymmetric short stature
n1=dysplasie acromicrique | n2=en:asymmetric short stature | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:charcot-marie-tooth disease, axonal, type 2e (disorder)
n1=dysplasie acromicrique | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:congenital deformity of left hand
n1=dysplasie acromicrique | n2=en:congenital deformity of left hand | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:dentin dyspalsia, shields type 2
n1=dysplasie acromicrique | n2=en:dentin dyspalsia, shields type 2 | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:disproportionate short stature
n1=dysplasie acromicrique | n2=en:disproportionate short stature | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:dystonia 12
n1=dysplasie acromicrique | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:hyperparathyroidism-jaw tumor syndrome
n1=dysplasie acromicrique | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:keratoacanthoma familial
n1=dysplasie acromicrique | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:longitudinal deficiency of tarsal bone
n1=dysplasie acromicrique | n2=en:longitudinal deficiency of tarsal bone | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:mainzer-saldino disease
n1=dysplasie acromicrique | n2=en:mainzer-saldino disease | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:maroteaux-lamy syndrome
n1=dysplasie acromicrique | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:microstomia
n1=dysplasie acromicrique | n2=en:microstomia | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:spondylocamptodactyly
n1=dysplasie acromicrique | n2=en:spondylocamptodactyly | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 26 / 0.619 ->
en:turcot syndrome
n1=dysplasie acromicrique | n2=en:turcot syndrome | rel=r_associated | relid=0 | w=26
- dysplasie acromicrique --
r_associated #0: 20 / 0.476 ->
en:Moore-Federman's syndrome
n1=dysplasie acromicrique | n2=en:Moore-Federman's syndrome | rel=r_associated | relid=0 | w=20
- dysplasie acromicrique --
r_associated #0: 20 / 0.476 ->
Moore-Federman (syndrome de)
n1=dysplasie acromicrique | n2=Moore-Federman (syndrome de) | rel=r_associated | relid=0 | w=20
- dysplasie acromicrique --
r_associated #0: 20 / 0.476 ->
syndrome de moore-federman
n1=dysplasie acromicrique | n2=syndrome de moore-federman | rel=r_associated | relid=0 | w=20
- dysplasie acromicrique --
r_associated #0: 9 / 0.214 ->
acromicrique
n1=dysplasie acromicrique | n2=acromicrique | rel=r_associated | relid=0 | w=9
- dysplasie acromicrique --
r_associated #0: 1 / 0.024 ->
en:dysplasia
n1=dysplasie acromicrique | n2=en:dysplasia | rel=r_associated | relid=0 | w=1
| ≈ 555 relations entrantes
- syndrome de Moore-Federman ---
r_associated #0: 35 -->
dysplasie acromicrique
n1=syndrome de Moore-Federman | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=35
- syndrome de moore-federman ---
r_associated #0: 35 -->
dysplasie acromicrique
n1=syndrome de moore-federman | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=35
- en:Moore-Federman's syndrome ---
r_associated #0: 31 -->
dysplasie acromicrique
n1=en:Moore-Federman's syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=31
- en:acromicric dysplasia ---
r_associated #0: 28 -->
dysplasie acromicrique
n1=en:acromicric dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=28
- Moore-Federman (syndrome de) ---
r_associated #0: 27 -->
dysplasie acromicrique
n1=Moore-Federman (syndrome de) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=27
- dysplasie ---
r_associated #0: 24 -->
dysplasie acromicrique
n1=dysplasie | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=24
- congenital ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=congenital | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- dysplasie géléophysique ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=dysplasie géléophysique | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- démence fronto-temporale ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=démence fronto-temporale | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:aberrant intrinsic muscles of hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:aberrant intrinsic muscles of hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:abnormal palmar creases ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:abnormal palmar creases | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:abnormal plantar creases ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:abnormal plantar creases | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:abnormally short growth ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:abnormally short growth | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:achondrogenesis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:achondrogenesis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:acrodysostosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:acrodysostosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:acute intermittent porphyria ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:acute intermittent porphyria | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:adult onset autosomal dominant leukodystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:adult onset autosomal dominant leukodystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:advanced sleep-phase syndrome, familial ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:advanced sleep-phase syndrome, familial | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:alagille syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:alagille syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:albright's hereditary osteodystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:albright's hereditary osteodystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:alpha-fetoprotein, hereditary persistence of ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:alpha-fetoprotein, hereditary persistence of | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:amelogenesis imperfecta, type ib ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:amelogenesis imperfecta, type ib | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ameloonychohypohidrotic syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ameloonychohypohidrotic syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:andersen syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:andersen syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:anteverted nostril ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:anteverted nostril | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:antley-bixler syndrome, autosomal dominant ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:antley-bixler syndrome, autosomal dominant | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:aplasia of lacrimal and salivary glands ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:aplasia of lacrimal and salivary glands | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:arthrogryposis multiplex congenita, neurogenic type (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:arthrogryposis, distal, type 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:arthrogryposis, distal, type 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:asexual dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:asexual dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:asymmetric short stature ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:asymmetric short stature | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:atelosteogenesis, type 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:atelosteogenesis, type 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:auriculo-condylar syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:auriculo-condylar syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autoimmune lymphoproliferative syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autoimmune lymphoproliferative syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant analbuminemia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant analbuminemia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant charcot-marie-tooth disease type 2a1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant charcot-marie-tooth disease type 2c ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant cystoid macular edema ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant cystoid macular edema | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant deficiency of plasminogen ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant deficiency of plasminogen | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant epidermolysis bullosa simplex ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant epidermolysis bullosa simplex | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant excess of transthyretin ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant excess of transthyretin | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant familial woolly hair ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant familial woolly hair | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant hyperinsulinism due to kir6.2 deficiency ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant hyperinsulinism due to sur1 deficiency ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant hypophosphatemic bone disease ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant hypophosphatemic bone disease | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant ichthyosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant ichthyosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant ichthyosis vulgaris ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant ichthyosis vulgaris | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant idiopathic familial dystonia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant idiopathic familial dystonia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant inheritance ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant inheritance | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant late onset basal ganglia degeneration ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant late onset basal ganglia degeneration | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant muscular dystrophy not predominantly limb girdle ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant mutilating keratoderma ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant mutilating keratoderma | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant oculocutaneous albinism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant oculocutaneous albinism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant optic atrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant optic atrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant polycystic kidney disease ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant polycystic kidney disease | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant progressive nephropathy with hypertension ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant progressive nephropathy with hypertension | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant pterygium of conjunctiva ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant pterygium of conjunctiva | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant retinitis pigmentosa ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant retinitis pigmentosa | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal dominant variant form of albumin ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal dominant variant form of albumin | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal recessive distal osteolysis syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal recessive distal osteolysis syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:autosomal recessive muscular dystrophy with limb girdle distribution ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:avascular necrosis of femoral head ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:avascular necrosis of femoral head | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:baller-gerold syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:baller-gerold syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:bannayan syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:bannayan syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:beare-stevenson cutis gyrata syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:beare-stevenson cutis gyrata syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:becker generalized myotonia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:becker generalized myotonia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:behavioral variant of frontotemporal dementia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:behavioral variant of frontotemporal dementia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:benign autosomal dominant osteopetrosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:benign autosomal dominant osteopetrosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:benign congenital myopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:benign congenital myopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:bilateral multiple fibroadenoma of breast ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:bilateral multiple fibroadenoma of breast | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:bilateral pheochromocytoma and islet cell adenoma of the pancreas ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:birth length less than 3rd percentile ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:birth length less than 3rd percentile | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:blau syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:blau syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:bone development disorder ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:bone development disorder | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachydactyly of hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachydactyly of hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachydactyly of toes ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachydactyly of toes | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachydactyly syndrome type b ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachydactyly syndrome type b | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachydactyly syndrome type c ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachydactyly syndrome type c | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachydactyly syndrome type e ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachydactyly syndrome type e | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachydactyly type a6 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachydactyly type a6 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachydactyly, type a1 (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachydactyly, type a1 (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachymesophalangy 2 and 5 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachymesophalangy 2 and 5 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachymetatarsia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachymetatarsia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachyolmia type 3 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachyolmia type 3 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brachyphalangia of toe ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brachyphalangia of toe | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brody myopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brody myopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:brooke-spiegler syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:brooke-spiegler syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:bulbous nose ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:bulbous nose | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cap myopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cap myopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:capillary malformation-arteriovenous malformation (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cataract, congenital, cerulean type 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cataract, congenital, cerulean type 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:centronuclear myopathy 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:centronuclear myopathy 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cerebral cavernous malformation ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cerebral cavernous malformation | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cerebral hemorrhage with amyloidosis, hereditary, dutch type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:char syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:char syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:charcot-marie-tooth disease type 2d ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:charcot-marie-tooth disease type 2d | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:charcot-marie-tooth disease, axonal, type 2b (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:charcot-marie-tooth disease, axonal, type 2e (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:charcot-marie-tooth disease, axonal, type 2l (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:charcot-marie-tooth disease, type 2j ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:charcot-marie-tooth disease, type 2j | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:chondrodysplasia punctata syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:chondrodysplasia punctata syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:chondrodysplasia, grebe type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:chondrodysplasia, grebe type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:choreoathetosis/spasticity, episodic ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:choreoathetosis/spasticity, episodic | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:chromosome 17q21.31 deletion syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:chromosome 17q21.31 deletion syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:chromosome 22q11.2 microduplication syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:chromosome 22q11.2 microduplication syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:chromosome 3q29 deletion syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:chromosome 3q29 deletion syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:chronic infantile neurological cutaneous and articular syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:chronic infantile neurological cutaneous and articular syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cleidocranial dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cleidocranial dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cochleosaccular degeneration of the inner ear and progressive cataracts ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:col1a1 associated connective tissue disorder ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:col1a1 associated connective tissue disorder | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cole disease ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cole disease | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cone-shaped epiphysis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cone-shaped epiphysis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital absence of foot ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital absence of foot | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital absence of hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital absence of hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of finger ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital anomaly of finger | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of metacarpal bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital anomaly of metacarpal bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of metatarsal bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital anomaly of metatarsal bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of tarsal bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital anomaly of tarsal bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of toe ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital anomaly of toe | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital bowing of long bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital bowing of long bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital claw foot ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital claw foot | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital deformity of left hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital deformity of left hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital deformity of right hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital deformity of right hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital dyserythropoietic anemia, type iii ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital dyserythropoietic anemia, type iii | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital finger deformity ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital finger deformity | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital foot deformity ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital foot deformity | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital hand agenesis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital hand agenesis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital hereditary muscular dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital hereditary muscular dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital malformation of thumb ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital malformation of thumb | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndromes associated with short stature ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital malformation syndromes associated with short stature | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital nephrogenic diabetes insipidus ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital nephrogenic diabetes insipidus | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital overgrowth of foot ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital overgrowth of foot | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital reticular ichthyosiform erythroderma ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital reticular ichthyosiform erythroderma | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital short achilles tendon ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital short achilles tendon | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital short quadriceps ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital short quadriceps | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital shortening of upper arm ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital shortening of upper arm | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital spade-like hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital spade-like hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital subluxation of carpus ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital subluxation of carpus | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital talipes varus ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital talipes varus | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:congenital valgus deformity of foot ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:congenital valgus deformity of foot | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:corneal dystrophy, congenital stromal ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:corneal dystrophy, congenital stromal | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:craniodiaphyseal dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:craniodiaphyseal dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cranioectodermal dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cranioectodermal dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:craniofacial deafness hand syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:craniofacial deafness hand syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:crouzon syndrome with acanthosis nigricans (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:currarino triad ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:currarino triad | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cutis laxa, autosomal dominant ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cutis laxa, autosomal dominant | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cutis laxa, autosomal recessive ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cutis laxa, autosomal recessive | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:cystinosis, infantile nephropathic ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:cystinosis, infantile nephropathic | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:de sanctis-cacchione syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:de sanctis-cacchione syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:deafness-craniofacial syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:deafness-craniofacial syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:deep philtrum ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:deep philtrum | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:deformity of digit of hand due to amniotic band ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:deformity of digit of hand due to amniotic band | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:delayed bone age ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:delayed bone age | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dentatorubral-pallidoluysian atrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dentatorubral-pallidoluysian atrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dentin dyspalsia, shields type 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dentin dyspalsia, shields type 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:diastrophic dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:diastrophic dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dicer1 syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dicer1 syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:diplopodia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:diplopodia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:disproportionate short stature ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:disproportionate short stature | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:distal arthrogryposis syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:distal arthrogryposis syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dolichocephalic dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dolichocephalic dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dominant autosomal hereditary disorder, complete penetrance ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dominant autosomal hereditary disorder, incomplete penetrance ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dominant beta-thalassemia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dominant beta-thalassemia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:donohue syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:donohue syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dopa-responsive dystonia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dopa-responsive dystonia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:duplication of the whole foot ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:duplication of the whole foot | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:duplication of whole hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:duplication of whole hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dwarfism, alopecia, pseudoanodontia, cutis laxa ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dwarfism, alopecia, pseudoanodontia, cutis laxa | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dyskeratosis congenita, autosomal dominant ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dyskeratosis congenita, autosomal dominant | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dysostosis multiplex group ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dysostosis multiplex group | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dysplasia, saddan ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dysplasia, saddan | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dyssegmental dysplasia with glaucoma syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dyssegmental dysplasia with glaucoma syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dystonia 12 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dystonia 12 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:dystrophia myotonica 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:dystrophia myotonica 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ectodermal dysplasia with natal teeth, turnpenny type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ectodermal dysplasia/ skin fragility syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ectrodactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ectrodactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ehlers-danlos syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ehlers-danlos syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ehlers-danlos syndrome, type i ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ehlers-danlos syndrome, type i | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:epidermolysis bullosa simplex with pyloric atresia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:epilepsy, myoclonic, benign adult familial, type 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:epiphyseal dysplasia, multiple, 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:epiphyseal dysplasia, multiple, 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:episodic ataxia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:episodic ataxia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:epithelial recurrent erosion dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:epithelial recurrent erosion dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial amyloid neuropathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial amyloid neuropathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial amyloid polyneuropathy, type v ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial amyloid polyneuropathy, type v | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial arthrogryposis-cholestatic hepatorenal syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial arthrogryposis-cholestatic hepatorenal syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial benign neonatal epilepsy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial benign neonatal epilepsy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial creutzfeldt-jakob ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial creutzfeldt-jakob | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial digital arthropathy and brachydactyly syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial digital arthropathy and brachydactyly syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial encephalopathy with neuroserpin inclusion bodies ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial hemiplegic migraine ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial hemiplegic migraine | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial hypercalciuric hypocalcemia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial hypercalciuric hypocalcemia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial hypodontia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial hypodontia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial interstitial nephritis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial interstitial nephritis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial isolated arrhythmogenic right ventricular dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial non-autoimmune autosomal dominant hyperthyroidism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial osteochondritis dissecans ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial osteochondritis dissecans | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial partial lipodystrophy, type 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial partial lipodystrophy, type 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:familial spontaneous pneumothorax ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:familial spontaneous pneumothorax | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:farber lipogranulomatosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:farber lipogranulomatosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fbn1, 3-bp dup, nt5202 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fbn1, 3-bp dup, nt5202 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fbn1, ala1728thr ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fbn1, ala1728thr | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fbn1, ser1750arg ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fbn1, ser1750arg | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fbn1, tyr1699cys ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fbn1, tyr1699cys | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fbn1, tyr1700cys ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fbn1, tyr1700cys | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:feingold syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:feingold syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:femur bifid with monodactylous ectrodactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:femur bifid with monodactylous ectrodactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fibrodysplasia ossificans progressiva ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fibrodysplasia ossificans progressiva | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fibular hypoplasia and complex brachydactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fibular hypoplasia and complex brachydactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fifth metacarpal with ulnar notch ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fifth metacarpal with ulnar notch | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fleck corneal dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fleck corneal dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:foxg1 syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:foxg1 syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:freeman-sheldon syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:freeman-sheldon syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:fronto-facio-nasal dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:fronto-facio-nasal dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:frontotemporal dementia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:frontotemporal dementia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:frontotemporal dementia, chromosome 3-linked ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:frontotemporal dementia, chromosome 3-linked | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:gaze palsy, familial horizontal, with progressive scoliosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:geleophysic dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:geleophysic dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:generalized epilepsy and paroxysmal dyskinesia syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:generalized myotonia of thomsen ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:generalized myotonia of thomsen | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:geniospasm 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:geniospasm 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:genitopatellar syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:genitopatellar syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:geroderma osteodysplastica ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:geroderma osteodysplastica | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:giacci familial neurogenic acroosteolysis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:giacci familial neurogenic acroosteolysis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:glomuvenous malformations ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:glomuvenous malformations | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:glucose transporter protein type 1 deficiency syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:glucose transporter protein type 1 deficiency syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:glycogen storage disease 0, liver ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:glycogen storage disease 0, liver | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:glycogen storage disease type x ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:glycogen storage disease type x | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:glycogen storage disease, muscular form ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:glycogen storage disease, muscular form | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:goniodysgenesis-mental retardation-short stature syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:growth cartilage disorganized, with islands of cells and abnormal collagen arrangement ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:growth cartilage disorganized, with islands of cells and abnormal collagen arrangement | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:gurrieri sammito bellussi syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:gurrieri sammito bellussi syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hand deformities ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hand deformities | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hand foot uterus syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hand foot uterus syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:haspeslagh fryns muelenaere syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:haspeslagh fryns muelenaere syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hawkinsinuria ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hawkinsinuria | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:heide syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:heide syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary angioedema ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary angioedema | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary benign intraepithelial dyskeratosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary benign intraepithelial dyskeratosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary breast and ovarian cancer syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary breast and ovarian cancer syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary cerebral amyloid angiopathy, icelandic type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary cystatin c amyloid angiopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary cystatin c amyloid angiopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary diffuse gastric adenocarcinoma ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary diffuse gastric adenocarcinoma | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary elliptocytosis due to abnormal protein 4.1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary elliptocytosis due to abnormal protein 4.1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary elliptocytosis due to alpha spectrin defect ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary elliptocytosis due to alpha spectrin defect | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary elliptocytosis due to beta spectrin defect in self-association ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary elliptocytosis due to beta spectrin defect in self-association | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary elliptocytosis due to deficiency of protein 4.1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary elliptocytosis due to deficiency of protein 4.1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary gastrogenic lactose intolerance ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary gastrogenic lactose intolerance | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary motor and sensory neuropathy type i ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary motor and sensory neuropathy type i | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary mucosal leukokeratosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary mucosal leukokeratosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary multiple exostoses ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary multiple exostoses | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary myopathy with early respiratory failure ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary myopathy with early respiratory failure | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary nonpolyposis colorectal cancer ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary nonpolyposis colorectal cancer | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary oculoleptomeningeal amyloid angiopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary papillary renal cell carcinoma ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary papillary renal cell carcinoma | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary sensory autonomic neuropathy, type 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary stomatocytosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary stomatocytosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary systemic amyloidosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary systemic amyloidosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hereditary tubulointerstitial disorder ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hereditary tubulointerstitial disorder | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:heritable pulmonary arterial hypertension due to bmpr2 mutation ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hnsha due to triosephosphate isomerase deficiency ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hnsha due to triosephosphate isomerase deficiency | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hoarseness ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hoarseness | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly with fetal akinesia-hypokinesia sequence ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hunter-thompson dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hunter-thompson dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyaline dystrophy of bruch's membrane ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyaline dystrophy of bruch's membrane | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyperferritinemia, hereditary, with congenital cataracts ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyperinsulinemic hypoglycemia, familial, 6 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyperinsulinemic hypoglycemia, familial, 6 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyperinsulinemic hypoglycemia, familial, 7 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyperinsulinism due to deficiency of glucokinase ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyperinsulinism due to deficiency of glucokinase | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyperinsulinism due to hnf4a deficiency ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyperinsulinism due to hnf4a deficiency | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hypermobility syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hypermobility syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyperparathyroidism-jaw tumor syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyperparathyroidism-jaw tumor syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hyperpigmentation, familial progressive ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hyperpigmentation, familial progressive | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hypophosphatemic rickets with hypercalciuria, hereditary ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hypoplastic tibia and postaxial polydactyly syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hypothyroid dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hypothyroid dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:hypotrichosis simplex of scalp ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:hypotrichosis simplex of scalp | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:idiopathic short stature ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:idiopathic short stature | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:infantile dwarf ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:infantile dwarf | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:inherited arthrogryposis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:inherited arthrogryposis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:insulin autoimmune syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:insulin autoimmune syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:insulin growth factor i resistance ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:insulin growth factor i resistance | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:internal notch of femoral head ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:internal notch of femoral head | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:iris coloboma with ptosis, hypertelorism, and mental retardation ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:jackson-weiss syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:jackson-weiss syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:jeune syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:jeune syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:kbg syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:kbg syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:keratitis, hereditary ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:keratitis, hereditary | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:keratoacanthoma familial ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:keratoacanthoma familial | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:keratosis palmoplantaris papulosa ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:keratosis palmoplantaris papulosa | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:klippel-feil syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:klippel-feil syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:klippel-trenaunay-weber syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:klippel-trenaunay-weber syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:knobloch syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:knobloch syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:kuskokwim disease ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:kuskokwim disease | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:lamellar ichthyosis, autosomal dominant form ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:lamellar ichthyosis, autosomal dominant form | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:laron syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:laron syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:laurin-sandrow syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:laurin-sandrow syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:leopard syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:leopard syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:lethal congenital contracture syndrome 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:lethal congenital contracture syndrome 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:lethal congenital contracture syndrome 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:lethal congenital contracture syndrome 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:lethal congenital contracture syndrome type 3 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:lethal congenital contracture syndrome type 3 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:li-fraumeni syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:li-fraumeni syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:liddle syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:liddle syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:limb deformities, congenital ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:limb deformities, congenital | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:lissencephaly syndrome, norman-roberts type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:lissencephaly syndrome, norman-roberts type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:loeys-dietz syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:loeys-dietz syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:long eyelashes ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:long eyelashes | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:long philtrum ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:long philtrum | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of carpal bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of carpal bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of femur ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of femur | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of humerus ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of humerus | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of left femur ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of left femur | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of left fibula ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of left fibula | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of metacarpal bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of metacarpal bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of phalanges of hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of phalanges of hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of radius ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of radius | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of tarsal bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of tarsal bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of tibia and/or fibula ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of tibia and/or fibula | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:longitudinal deficiency of ulna ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:longitudinal deficiency of ulna | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:lynch syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:lynch syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:macdermot winter syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:macdermot winter syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:macrodactyly of the hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:macrodactyly of the hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:macular corneal dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:macular corneal dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mainzer-saldino disease ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mainzer-saldino disease | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:majeed syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:majeed syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mandibuloacral dysplasia with type a lipodystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:marden-walker syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:marden-walker syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:marfan syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:marfan syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:maroteaux-lamy syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:maroteaux-lamy syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mauriac's syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mauriac's syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:may-hegglin anomaly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:may-hegglin anomaly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:melanoma astrocytoma syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:melanoma astrocytoma syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:melnick-fraser syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:melnick-fraser syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:menkes disease ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:menkes disease | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mesomelic dwarfism reinhardt pfeiffer type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:metaphyseal dysplasia, braun-tinschert type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:metaphyseal dysplasia, braun-tinschert type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:metatropic dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:metatropic dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:microcephaly cervical spine fusion anomalies ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:microcephaly cervical spine fusion anomalies | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:microcephaly deafness syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:microcephaly deafness syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:microcornea with glaucoma and absent frontal sinus syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:microphthalmia, syndromic 3 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:microphthalmia, syndromic 3 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:microstomia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:microstomia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mild facial anomalies ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mild facial anomalies | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:miller-mckusick-malvaux-syndrome (3m syndrome) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mitochondrial neurogastrointestinal encephalomyopathy syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:morquio syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:morquio syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mowat-wilson syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mowat-wilson syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:muckle-wells syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:muckle-wells syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:mullerian duct and limb anomalies syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:mullerian duct and limb anomalies syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:multicentric osteolysis nodulosis arthropathy spectrum ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:multiple endocrine neoplasia type 2b ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:multiple endocrine neoplasia type 2b | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:multiple epiphyseal dysplasia type 5 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:multiple epiphyseal dysplasia type 5 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:muscle amp deaminase deficiency ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:muscle amp deaminase deficiency | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:muscle l-lactate dehydrogenase deficiency ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:muscle l-lactate dehydrogenase deficiency | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:myhre syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:myhre syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:myopathy with abnormal lipid metabolism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:myopathy with abnormal lipid metabolism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:myopathy with exercise intolerance, swedish type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:myopathy with exercise intolerance, swedish type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:myopathy, distal 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:myopathy, distal 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:myopathy, distal, tateyama type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:myopathy, distal, tateyama type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:nail-patella syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:nail-patella syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:nathalie syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:nathalie syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:nemaline myopathy 3 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:nemaline myopathy 3 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:neurofibromatosis type 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:neurofibromatosis type 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:neurofibromatosis type 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:neurofibromatosis type 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:neurofibromatosis, type 1-like syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:neurofibromatosis, type 1-like syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:neuropathy, hereditary motor and sensory, okinawa type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:neuropathy, hereditary thermosensitive ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:neuropathy, hereditary thermosensitive | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:nevoid basal cell carcinoma syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:nevoid basal cell carcinoma syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:nicolaides baraitser syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:nicolaides baraitser syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:non-dystrophic myotonia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:non-dystrophic myotonia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:nonaka myopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:nonaka myopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:noonan syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:noonan syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:nutritional stunting ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:nutritional stunting | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:o/e - short stature ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:o/e - short stature | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:oculodental syndrome rutherfurd syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:oculodental syndrome rutherfurd syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:okihiro syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:okihiro syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, levin type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:osteogenesis imperfecta, levin type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:otoonychoperoneal syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:otoonychoperoneal syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ovoid vertebral bodies ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ovoid vertebral bodies | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:papillon-lefevre syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:papillon-lefevre syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:parietal foramina ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:parietal foramina | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:paroxysmal extreme pain disorder ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:paroxysmal extreme pain disorder | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:peripheral resistance to thyroid hormone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:peripheral resistance to thyroid hormone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:peutz-jeghers syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:peutz-jeghers syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:piebaldism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:piebaldism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pitt-hopkins syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pitt-hopkins syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pituitary adenoma, familial isolated (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pituitary adenoma, familial isolated (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pituitary dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pituitary dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:plantarflexed cuboid ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:plantarflexed cuboid | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:polydactyly, preaxial ii (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:polydactyly, preaxial ii (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:polyostotic fibrous dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:polyostotic fibrous dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:popliteal pterygium syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:popliteal pterygium syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:potassium aggravated myotonia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:potassium aggravated myotonia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:potocki-shaffer syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:potocki-shaffer syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:prader-willi habitus, osteopenia, and camptodactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:primary hypertrophic osteoarthropathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:primary hypertrophic osteoarthropathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:proportionate short stature ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:proportionate short stature | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:proteus-like syndrome (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:proteus-like syndrome (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:prune belly syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:prune belly syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pseudocholinesterase deficiency ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pseudocholinesterase deficiency | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pseudohypoaldosteronism, type 1, dominant form ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pseudohypoparathyroidism and pseudopseudohypoparathyroidism type i ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pseudohypoparathyroidism and pseudopseudohypoparathyroidism type i | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pseudomuscular build ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pseudomuscular build | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pulmonary interstitial glycogenosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pulmonary interstitial glycogenosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:pyle metaphyseal dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:pyle metaphyseal dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:rachitic dwarf ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:rachitic dwarf | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:radial aplasia-thrombocytopenia syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:radial aplasia-thrombocytopenia syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:radial hypoplasia, triphalangeal thumbs and hypospadias ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:reardon hall slaney syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:reardon hall slaney syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:reis-bucklers' corneal dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:reis-bucklers' corneal dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:renal dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:renal dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:reticulate acropigmentation of kitamura ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:reticulate acropigmentation of kitamura | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:rhizomelic chondrodysplasia punctata ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:rhizomelic chondrodysplasia punctata | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:robinow syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:robinow syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:roch leri mesosomatous lipomatosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:roch leri mesosomatous lipomatosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:round face ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:round face | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:rud syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:rud syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:saito kuba tsuruta syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:saito kuba tsuruta syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:schnyder crystalline corneal dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:schnyder crystalline corneal dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:sebastian syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:sebastian syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:second metacarpal notched proximally on radial side ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:second metacarpal notched proximally on radial side | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:sellars beighton syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:sellars beighton syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:senile dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:senile dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short foot ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short foot | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short long bone ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short long bone | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short palms ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short palms | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short stature associated with bone marrow transplant ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short stature associated with bone marrow transplant | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short stature co-occurrent and due to endocrine disorder ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short stature co-occurrent and due to endocrine disorder | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short stature due to radiation therapy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short stature due to radiation therapy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short stature with valvular heart disease and characteristic facies syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short, stubby metacarpals ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short, stubby metacarpals | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:short, stubby phalanges ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:short, stubby phalanges | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:shprintzen omphalocele syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:shprintzen omphalocele syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:shwachman-diamond syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:shwachman-diamond syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:smith-mccort dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:smith-mccort dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 10 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia 10 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 1s ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia 1s | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 28 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia 28 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 29 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia 29 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 31 (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia 31 (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 36 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia 36 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 8 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia 8 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia type 2 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia type 2 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia type 4 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia type 4 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia type 5 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia type 5 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia type 6 (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia type 6 (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia type 7 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spinocerebellar ataxia type 7 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:split foot ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:split foot | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:split-hand-foot malformation with long bone deficiency 1 ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondylo-ocular syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondylo-ocular syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondylocamptodactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondylocamptodactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondylocostal dysostosis 4, autosomal dominant ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondyloenchondrodysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondyloenchondrodysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondyloenchondrodysplasia with immune dysregulation ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondyloepiphyseal dysplasia tarda, toledo type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondyloepiphyseal dysplasia tarda, x-linked ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondyloepiphyseal dysplasia tarda, x-linked | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondyloepiphyseal dysplasia, omani type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondyloepiphyseal dysplasia, omani type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:spondyloperipheral dysplasia short ulna ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:spondyloperipheral dysplasia short ulna | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:steatocystoma multiplex ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:steatocystoma multiplex | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:steinfeld syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:steinfeld syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:stickler syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:stickler syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:sting-associated vasculopathy with onset in infancy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:sting-associated vasculopathy with onset in infancy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:strudwick syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:strudwick syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:symbrachydactyly of toe ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:symbrachydactyly of toe | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:syndactyly, type i ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:syndactyly, type i | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:syndactyly, type iii ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:syndactyly, type iii | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:syndrome, branchio-oculo-facial ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:syndrome, branchio-oculo-facial | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:syndromic orbital border hypoplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:syndromic orbital border hypoplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:synpolydactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:synpolydactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:tarsal coalitions ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:tarsal coalitions | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:tarsal-carpal coalition syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:tarsal-carpal coalition syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:thanatophoric dysplasia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:thanatophoric dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:thick skin ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:thick skin | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:thick vermilion border ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:thick vermilion border | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:thiel-behnke corneal dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:thiel-behnke corneal dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:tmem70 related mitochondrial encephalo-cardio-myopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:transthyretin related familial amyloid cardiomyopathy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:transthyretin related familial amyloid cardiomyopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:transverse deficiency of hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:transverse deficiency of hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:treacher collins syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:treacher collins syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:triglyceride storage disease with ichthyosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:triglyceride storage disease with ichthyosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:tryptophanuria with dwarfism ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:tryptophanuria with dwarfism | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:turcot syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:turcot syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:tylosis ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:tylosis | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:type i acrocephalosyndactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:type i acrocephalosyndactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:type ii acrocephalopolysyndactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:type ii acrocephalopolysyndactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:type v acrocephalosyndactyly ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:type v acrocephalosyndactyly | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ulna metaphyseal dysplasia syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ulna metaphyseal dysplasia syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ulnar dimelia ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ulnar dimelia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:ulnar-mammary syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:ulnar-mammary syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:undergrowth of whole hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:undergrowth of whole hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:verloes bourguignon syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:verloes bourguignon syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:vitelliform macular dystrophy ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:vitelliform macular dystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:vitreoretinochoroidopathy (disorder) ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:vitreoretinochoroidopathy (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:von willebrand disease, platelet type ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:von willebrand disease, platelet type | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:well-defined eyebrows ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:well-defined eyebrows | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:wellesley carman french syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:wellesley carman french syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:wells jankovic syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:wells jankovic syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:whyte hemingway carpal tarsal phalangeal osteolyses ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:whyte hemingway carpal tarsal phalangeal osteolyses | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:windblown hand ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:windblown hand | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:wnt4 mullerian aplasia and ovarian dysfunction ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- en:zimmerman laband syndrome ---
r_associated #0: 20 -->
dysplasie acromicrique
n1=en:zimmerman laband syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
- aclasie diaphysaire ---
r_associated #0: 15 -->
dysplasie acromicrique
n1=aclasie diaphysaire | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=15
- chondrodysplasie héréditaire déformante ---
r_associated #0: 15 -->
dysplasie acromicrique
n1=chondrodysplasie héréditaire déformante | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=15
- exostose héréditaire multiple ---
r_associated #0: 15 -->
dysplasie acromicrique
n1=exostose héréditaire multiple | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=15
- arachnodactylie ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=arachnodactylie | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- chondrodysplasie déformante héréditaire ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=chondrodysplasie déformante héréditaire | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:Albright's hereditary osteodystrophy ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:Albright's hereditary osteodystrophy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:Ehlers-Danlos syndrome ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:Ehlers-Danlos syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:Feingold syndrome ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:Feingold syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:LEOPARD syndrome ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:LEOPARD syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:Marden-Walker syndrome ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:Marden-Walker syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:Peutz-Jeghers syndrome ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:Peutz-Jeghers syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:Pitt-Hopkins syndrome ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:Pitt-Hopkins syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:dysplasia ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:dysplasia | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:eds ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:eds | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- en:ehlers danlos syndrome ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=en:ehlers danlos syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- maladie de Bessel-Hagen ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=maladie de Bessel-Hagen | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- maladie exostosante multiple ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=maladie exostosante multiple | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- maladie ostéogénique ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=maladie ostéogénique | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- nanisme ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=nanisme | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- nanisme diastrophique ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=nanisme diastrophique | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- piebaldisme ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=piebaldisme | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- piébaldisme ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=piébaldisme | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- steatocystoma multiplex ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=steatocystoma multiplex | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- stéatocystomes multiples ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=stéatocystomes multiples | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- syndrome d'hyperparathyroïdie et tumeur de la mâchoire ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=syndrome d'hyperparathyroïdie et tumeur de la mâchoire | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- syndrome héréditaire de cancer du sein et de l'ovaire ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire ---
r_associated #0: 10 -->
dysplasie acromicrique
n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=10
- maladie des exostoses multiples ---
r_associated #0: 5 -->
dysplasie acromicrique
n1=maladie des exostoses multiples | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=5
- neuropathie sensitive héréditaire dominante de type i ---
r_associated #0: 5 -->
dysplasie acromicrique
n1=neuropathie sensitive héréditaire dominante de type i | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=5
- pied bifide ---
r_associated #0: 5 -->
dysplasie acromicrique
n1=pied bifide | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=5
- syndrome d'Ehlers-Danlos ---
r_associated #0: 5 -->
dysplasie acromicrique
n1=syndrome d'Ehlers-Danlos | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=5
- syndrome de Stickler ---
r_associated #0: 5 -->
dysplasie acromicrique
n1=syndrome de Stickler | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=5
- syndrome lymphoprolifératif avec autoimmunité ---
r_associated #0: 5 -->
dysplasie acromicrique
n1=syndrome lymphoprolifératif avec autoimmunité | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=5
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