'en:orofaciodigital syndromes'
(id=6862297 ; fe=en:orofaciodigital syndromes ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=16626 creation date=2017-06-25 touchdate=2025-08-27 16:50:54.000) ≈ 253 relations sortantes
- en:orofaciodigital syndromes --
r_associated #0: 43 / 1 ->
en:genetic diseases, x-linked
n1=en:orofaciodigital syndromes | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=43
- en:orofaciodigital syndromes --
r_associated #0: 42 / 0.977 ->
en:nutritional management
n1=en:orofaciodigital syndromes | n2=en:nutritional management | rel=r_associated | relid=0 | w=42
- en:orofaciodigital syndromes --
r_associated #0: 42 / 0.977 ->
en:prune belly syndrome
n1=en:orofaciodigital syndromes | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=42
- en:orofaciodigital syndromes --
r_associated #0: 42 / 0.977 ->
en:zellweger syndrome
n1=en:orofaciodigital syndromes | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=42
- en:orofaciodigital syndromes --
r_associated #0: 40 / 0.93 ->
en:historical aspects qualifier
n1=en:orofaciodigital syndromes | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=40
- en:orofaciodigital syndromes --
r_associated #0: 40 / 0.93 ->
en:in blood
n1=en:orofaciodigital syndromes | n2=en:in blood | rel=r_associated | relid=0 | w=40
- en:orofaciodigital syndromes --
r_associated #0: 39 / 0.907 ->
en:microcephaly
n1=en:orofaciodigital syndromes | n2=en:microcephaly | rel=r_associated | relid=0 | w=39
- en:orofaciodigital syndromes --
r_associated #0: 38 / 0.884 ->
en:viruses
n1=en:orofaciodigital syndromes | n2=en:viruses | rel=r_associated | relid=0 | w=38
- en:orofaciodigital syndromes --
r_associated #0: 36 / 0.837 ->
en:complication aspects
n1=en:orofaciodigital syndromes | n2=en:complication aspects | rel=r_associated | relid=0 | w=36
- en:orofaciodigital syndromes --
r_associated #0: 36 / 0.837 ->
en:enzymology
n1=en:orofaciodigital syndromes | n2=en:enzymology | rel=r_associated | relid=0 | w=36
- en:orofaciodigital syndromes --
r_associated #0: 36 / 0.837 ->
en:nevoid basal cell carcinoma syndrome
n1=en:orofaciodigital syndromes | n2=en:nevoid basal cell carcinoma syndrome | rel=r_associated | relid=0 | w=36
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
dysmorphies des freins buccaux
n1=en:orofaciodigital syndromes | n2=dysmorphies des freins buccaux | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:acrodysostosis
n1=en:orofaciodigital syndromes | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:beckwith-wiedemann syndrome
n1=en:orofaciodigital syndromes | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:charge syndrome
n1=en:orofaciodigital syndromes | n2=en:charge syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:cockayne syndrome
n1=en:orofaciodigital syndromes | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:congenital abnormal synostosis
n1=en:orofaciodigital syndromes | n2=en:congenital abnormal synostosis | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:craniofacial dysostosis
n1=en:orofaciodigital syndromes | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:ectodermal dysplasia
n1=en:orofaciodigital syndromes | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:holoprosencephaly
n1=en:orofaciodigital syndromes | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:in cerebrospinal fluid
n1=en:orofaciodigital syndromes | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:mobius syndrome
n1=en:orofaciodigital syndromes | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:orofaciodigital syndrome 11
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 11 | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:orofaciodigital syndrome 4
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 4 | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:orofaciodigital syndrome 8
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 8 | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:proteus syndrome
n1=en:orofaciodigital syndromes | n2=en:proteus syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:smith-magenis syndrome
n1=en:orofaciodigital syndromes | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:weill-marchesani syndrome
n1=en:orofaciodigital syndromes | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
en:wolf-hirschhorn syndrome
n1=en:orofaciodigital syndromes | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
syndrome oro-digito-facial
n1=en:orofaciodigital syndromes | n2=syndrome oro-digito-facial | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
syndrome orodigitofacial
n1=en:orofaciodigital syndromes | n2=syndrome orodigitofacial | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 35 / 0.814 ->
syndromes oro-facio-digitaux
n1=en:orofaciodigital syndromes | n2=syndromes oro-facio-digitaux | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:barth syndrome
n1=en:orofaciodigital syndromes | n2=en:barth syndrome | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:costello syndrome
n1=en:orofaciodigital syndromes | n2=en:costello syndrome | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:exposure as collected domain
n1=en:orofaciodigital syndromes | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:in urine
n1=en:orofaciodigital syndromes | n2=en:in urine | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:metabolic aspects
n1=en:orofaciodigital syndromes | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:orofaciodigital syndrome 5
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 5 | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:pentalogy of cantrell
n1=en:orofaciodigital syndromes | n2=en:pentalogy of cantrell | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:physiopathological
n1=en:orofaciodigital syndromes | n2=en:physiopathological | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:sotos syndrome
n1=en:orofaciodigital syndromes | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
en:surgical aspects
n1=en:orofaciodigital syndromes | n2=en:surgical aspects | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 34 / 0.791 ->
syndrome oro-facio-digital
n1=en:orofaciodigital syndromes | n2=syndrome oro-facio-digital | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:carney complex
n1=en:orofaciodigital syndromes | n2=en:carney complex | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:cleft lip/palate with abnormal thumbs and microcephaly
n1=en:orofaciodigital syndromes | n2=en:cleft lip/palate with abnormal thumbs and microcephaly | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:cleidocranial dysplasia
n1=en:orofaciodigital syndromes | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:congenital rubella
n1=en:orofaciodigital syndromes | n2=en:congenital rubella | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:epidemiologic
n1=en:orofaciodigital syndromes | n2=en:epidemiologic | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:laurence-moon syndrome
n1=en:orofaciodigital syndromes | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:maxillofacial abnormalities
n1=en:orofaciodigital syndromes | n2=en:maxillofacial abnormalities | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:noonan syndrome
n1=en:orofaciodigital syndromes | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:opitz g/bbb syndrome
n1=en:orofaciodigital syndromes | n2=en:opitz g/bbb syndrome | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:parasitology
n1=en:orofaciodigital syndromes | n2=en:parasitology | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:roentgenographic
n1=en:orofaciodigital syndromes | n2=en:roentgenographic | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:rubinstein-taybi syndrome
n1=en:orofaciodigital syndromes | n2=en:rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:russell-silver syndrome
n1=en:orofaciodigital syndromes | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:sex chromosome disorders of sex development
n1=en:orofaciodigital syndromes | n2=en:sex chromosome disorders of sex development | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:therapeutic aspects
n1=en:orofaciodigital syndromes | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 32 / 0.744 ->
en:x chromosome-linked pyridoxine refractory sideroblastic anemia
n1=en:orofaciodigital syndromes | n2=en:x chromosome-linked pyridoxine refractory sideroblastic anemia | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
dysmorphie des freins buccaux
n1=en:orofaciodigital syndromes | n2=dysmorphie des freins buccaux | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:22q11 deletion syndrome
n1=en:orofaciodigital syndromes | n2=en:22q11 deletion syndrome | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:donohue syndrome
n1=en:orofaciodigital syndromes | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:gardner syndrome
n1=en:orofaciodigital syndromes | n2=en:gardner syndrome | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:klippel-feil syndrome
n1=en:orofaciodigital syndromes | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:mandibuloacral dysplasia with type a lipodystrophy
n1=en:orofaciodigital syndromes | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:marfan syndrome
n1=en:orofaciodigital syndromes | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:ornithine carbamoyltransferase deficiency disease
n1=en:orofaciodigital syndromes | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:orofaciodigital syndrome 3
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 3 | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:orofaciodigital syndrome vii
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome vii | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:pallister-hall syndrome
n1=en:orofaciodigital syndromes | n2=en:pallister-hall syndrome | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:pharmacotherapeutic
n1=en:orofaciodigital syndromes | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:platybasia
n1=en:orofaciodigital syndromes | n2=en:platybasia | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:sex chromosome disorders
n1=en:orofaciodigital syndromes | n2=en:sex chromosome disorders | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:taxonomic
n1=en:orofaciodigital syndromes | n2=en:taxonomic | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 31 / 0.721 ->
en:use of ultrasonography
n1=en:orofaciodigital syndromes | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=31
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:angelman syndrome
n1=en:orofaciodigital syndromes | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:deaf-blind disorders
n1=en:orofaciodigital syndromes | n2=en:deaf-blind disorders | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:down syndrome
n1=en:orofaciodigital syndromes | n2=en:down syndrome | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:fronto-naso-ethmoidal dysostosis
n1=en:orofaciodigital syndromes | n2=en:fronto-naso-ethmoidal dysostosis | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:genetic aspects
n1=en:orofaciodigital syndromes | n2=en:genetic aspects | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:immunology aspects
n1=en:orofaciodigital syndromes | n2=en:immunology aspects | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:macrocephaly
n1=en:orofaciodigital syndromes | n2=en:macrocephaly | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:microbiological
n1=en:orofaciodigital syndromes | n2=en:microbiological | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:nursing therapy
n1=en:orofaciodigital syndromes | n2=en:nursing therapy | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:orofaciodigital syndrome 13
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 13 | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:orofaciodigital syndrome 9
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 9 | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:pathological aspects
n1=en:orofaciodigital syndromes | n2=en:pathological aspects | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:radiotherapeutic
n1=en:orofaciodigital syndromes | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 30 / 0.698 ->
en:short rib-polydactyly syndrome
n1=en:orofaciodigital syndromes | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:craniofacial abnormalities
n1=en:orofaciodigital syndromes | n2=en:craniofacial abnormalities | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:dysostosis of bone of skull
n1=en:orofaciodigital syndromes | n2=en:dysostosis of bone of skull | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:etiology aspects
n1=en:orofaciodigital syndromes | n2=en:etiology aspects | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:heterotaxy syndrome
n1=en:orofaciodigital syndromes | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:ischio-vertebral syndrome
n1=en:orofaciodigital syndromes | n2=en:ischio-vertebral syndrome | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:melnick-fraser syndrome
n1=en:orofaciodigital syndromes | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:monilethrix
n1=en:orofaciodigital syndromes | n2=en:monilethrix | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:nail-patella syndrome
n1=en:orofaciodigital syndromes | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:netherton syndrome
n1=en:orofaciodigital syndromes | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:organoid nevus
n1=en:orofaciodigital syndromes | n2=en:organoid nevus | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:orofaciodigital syndrome x
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome x | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:prader-willi syndrome
n1=en:orofaciodigital syndromes | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:spondylocostal dysostosis 4, autosomal dominant
n1=en:orofaciodigital syndromes | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 29 / 0.674 ->
en:veterinary aspects
n1=en:orofaciodigital syndromes | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=29
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:alstrom syndrome
n1=en:orofaciodigital syndromes | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:aspects of mortality statistics
n1=en:orofaciodigital syndromes | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:aspects of radionuclide imaging
n1=en:orofaciodigital syndromes | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:bloom syndrome
n1=en:orofaciodigital syndromes | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:diagnosis aspect
n1=en:orofaciodigital syndromes | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:incontinentia pigmenti
n1=en:orofaciodigital syndromes | n2=en:incontinentia pigmenti | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:juvenile x-linked retinoschisis
n1=en:orofaciodigital syndromes | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:leopard syndrome
n1=en:orofaciodigital syndromes | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:multiple congenital anomalies
n1=en:orofaciodigital syndromes | n2=en:multiple congenital anomalies | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:orofaciodigital syndrome 12
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome 12 | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 28 / 0.651 ->
en:trichothiodystrophy
n1=en:orofaciodigital syndromes | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=28
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
dysostoses oro-digito-faciales
n1=en:orofaciodigital syndromes | n2=dysostoses oro-digito-faciales | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:alagille syndrome
n1=en:orofaciodigital syndromes | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:bardet-biedl syndrome
n1=en:orofaciodigital syndromes | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:chemically induced
n1=en:orofaciodigital syndromes | n2=en:chemically induced | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:craniosynostosis
n1=en:orofaciodigital syndromes | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:ethnologic
n1=en:orofaciodigital syndromes | n2=en:ethnologic | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:fronto-frontal dysostosis
n1=en:orofaciodigital syndromes | n2=en:fronto-frontal dysostosis | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:orofaciodigital syndrome type 1
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:plagiocephaly
n1=en:orofaciodigital syndromes | n2=en:plagiocephaly | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:poems syndrome
n1=en:orofaciodigital syndromes | n2=en:poems syndrome | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:prolidase deficiency
n1=en:orofaciodigital syndromes | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:rehabilitation aspects
n1=en:orofaciodigital syndromes | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:smith-lemli-opitz syndrome
n1=en:orofaciodigital syndromes | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:syndrome, mohr
n1=en:orofaciodigital syndromes | n2=en:syndrome, mohr | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
en:waardenburg syndrome
n1=en:orofaciodigital syndromes | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 27 / 0.628 ->
syndrome de Marfan
n1=en:orofaciodigital syndromes | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=27
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:acrofacial dysostosis
n1=en:orofaciodigital syndromes | n2=en:acrofacial dysostosis | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:cri du chat syndrome
n1=en:orofaciodigital syndromes | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:dysostosis
n1=en:orofaciodigital syndromes | n2=en:dysostosis | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:embryologic
n1=en:orofaciodigital syndromes | n2=en:embryologic | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:focal dermal hypoplasia
n1=en:orofaciodigital syndromes | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:fragile x syndrome
n1=en:orofaciodigital syndromes | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:fraser syndrome
n1=en:orofaciodigital syndromes | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:isolated noncompaction of the ventricular myocardium
n1=en:orofaciodigital syndromes | n2=en:isolated noncompaction of the ventricular myocardium | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:loeys-dietz syndrome
n1=en:orofaciodigital syndromes | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:oculocerebrorenal syndrome
n1=en:orofaciodigital syndromes | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:orofaciodigital syndrome type 6
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:psychology qualifier
n1=en:orofaciodigital syndromes | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:spheno-frontal dysostosis
n1=en:orofaciodigital syndromes | n2=en:spheno-frontal dysostosis | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 26 / 0.605 ->
en:spondylocostal dysostosis
n1=en:orofaciodigital syndromes | n2=en:spondylocostal dysostosis | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndromes --
r_associated #0: 25 / 0.581 ->
syndromes
n1=en:orofaciodigital syndromes | n2=syndromes | rel=r_associated | relid=0 | w=25
- en:orofaciodigital syndromes --
r_associated #0: 24 / 0.558 ->
maladie de Marfan
n1=en:orofaciodigital syndromes | n2=maladie de Marfan | rel=r_associated | relid=0 | w=24
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
AFD de type Catania
n1=en:orofaciodigital syndromes | n2=AFD de type Catania | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
anomalies morphologiques maxillofaciales
n1=en:orofaciodigital syndromes | n2=anomalies morphologiques maxillofaciales | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
aplasie de la paroi abdominale
n1=en:orofaciodigital syndromes | n2=aplasie de la paroi abdominale | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
arachnodactylie
n1=en:orofaciodigital syndromes | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
chondrodysplasie léthale avec brièveté des côtes
n1=en:orofaciodigital syndromes | n2=chondrodysplasie léthale avec brièveté des côtes | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
crânio-sténose
n1=en:orofaciodigital syndromes | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
craniosténose
n1=en:orofaciodigital syndromes | n2=craniosténose | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
crâniosténose
n1=en:orofaciodigital syndromes | n2=crâniosténose | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
craniosynostose
n1=en:orofaciodigital syndromes | n2=craniosynostose | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
crâniosynostose
n1=en:orofaciodigital syndromes | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
déficit en prolidase
n1=en:orofaciodigital syndromes | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dysostose acrofaciale
n1=en:orofaciodigital syndromes | n2=dysostose acrofaciale | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dysostose craniofaciale
n1=en:orofaciodigital syndromes | n2=dysostose craniofaciale | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dysplasie cléido-crânienne
n1=en:orofaciodigital syndromes | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dysplasie cléidocrânienne
n1=en:orofaciodigital syndromes | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dysplasie ectodermique
n1=en:orofaciodigital syndromes | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
n1=en:orofaciodigital syndromes | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dysplasie ectodermique, ectrodactylie et dystrophie maculaire
n1=en:orofaciodigital syndromes | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
dystrophie orbitaire congénitale
n1=en:orofaciodigital syndromes | n2=dystrophie orbitaire congénitale | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
n1=en:orofaciodigital syndromes | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:and mental retardation
n1=en:orofaciodigital syndromes | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Angelman syndrome
n1=en:orofaciodigital syndromes | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:arachnodactily
n1=en:orofaciodigital syndromes | n2=en:arachnodactily | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:arachnodactyly
n1=en:orofaciodigital syndromes | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:basal cell nævus
n1=en:orofaciodigital syndromes | n2=en:basal cell nævus | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:basal cell nevus syndrome
n1=en:orofaciodigital syndromes | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:cerebral gigantism
n1=en:orofaciodigital syndromes | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:cleft lip and palate
n1=en:orofaciodigital syndromes | n2=en:cleft lip and palate | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:craniostenosis
n1=en:orofaciodigital syndromes | n2=en:craniostenosis | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
n1=en:orofaciodigital syndromes | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Donohue syndrome
n1=en:orofaciodigital syndromes | n2=en:Donohue syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Down syndrome
n1=en:orofaciodigital syndromes | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:fragile X syndrome
n1=en:orofaciodigital syndromes | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Goltz syndrome
n1=en:orofaciodigital syndromes | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:heterotaxy
n1=en:orofaciodigital syndromes | n2=en:heterotaxy | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Marfan's disease
n1=en:orofaciodigital syndromes | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:marfan's syndrome
n1=en:orofaciodigital syndromes | n2=en:marfan's syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Marfan's syndrome
n1=en:orofaciodigital syndromes | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:melhem fahl syndrome
n1=en:orofaciodigital syndromes | n2=en:melhem fahl syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:morava mehes syndrome
n1=en:orofaciodigital syndromes | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:onychoosteodysostosis
n1=en:orofaciodigital syndromes | n2=en:onychoosteodysostosis | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:orofaciodigital syndrome
n1=en:orofaciodigital syndromes | n2=en:orofaciodigital syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:pelviscapular dysplasia
n1=en:orofaciodigital syndromes | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:polydactyly, preaxial ii (disorder)
n1=en:orofaciodigital syndromes | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Prader-Willi syndrome
n1=en:orofaciodigital syndromes | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:preaxial deficiency, postaxial polydactyly and hypospadias
n1=en:orofaciodigital syndromes | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:progressive non-infectious anterior vertebral fusion
n1=en:orofaciodigital syndromes | n2=en:progressive non-infectious anterior vertebral fusion | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:situs inversus
n1=en:orofaciodigital syndromes | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:situs inversus viscerum
n1=en:orofaciodigital syndromes | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:situs mutatus
n1=en:orofaciodigital syndromes | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Soto's syndrome
n1=en:orofaciodigital syndromes | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Sotos' syndrome
n1=en:orofaciodigital syndromes | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:sotos' syndrome
n1=en:orofaciodigital syndromes | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome
n1=en:orofaciodigital syndromes | n2=en:tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:trisomy
n1=en:orofaciodigital syndromes | n2=en:trisomy | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
en:Zellweger syndrome
n1=en:orofaciodigital syndromes | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
enzymologie
n1=en:orofaciodigital syndromes | n2=enzymologie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
enzymology
n1=en:orofaciodigital syndromes | n2=enzymology | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
épidémiologique
n1=en:orofaciodigital syndromes | n2=épidémiologique | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
gigantisme cérébral
n1=en:orofaciodigital syndromes | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
Goltz
n1=en:orofaciodigital syndromes | n2=Goltz | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
hétérotaxie
n1=en:orofaciodigital syndromes | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie
n1=en:orofaciodigital syndromes | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie de type 2
n1=en:orofaciodigital syndromes | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie de type 3
n1=en:orofaciodigital syndromes | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie de type 4
n1=en:orofaciodigital syndromes | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie familiale alobaire de type 1
n1=en:orofaciodigital syndromes | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
hypoplasie dermique en aires
n1=en:orofaciodigital syndromes | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
hypoplasie dermique focale
n1=en:orofaciodigital syndromes | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
maladie de marfan
n1=en:orofaciodigital syndromes | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
malformations maxillo-faciales
n1=en:orofaciodigital syndromes | n2=malformations maxillo-faciales | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
malformations maxillofaciales
n1=en:orofaciodigital syndromes | n2=malformations maxillofaciales | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
microbiologique
n1=en:orofaciodigital syndromes | n2=microbiologique | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
monilethrix
n1=en:orofaciodigital syndromes | n2=monilethrix | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
naevomatose baso-cellulaire
n1=en:orofaciodigital syndromes | n2=naevomatose baso-cellulaire | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
naevomatose basocellulaire
n1=en:orofaciodigital syndromes | n2=naevomatose basocellulaire | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
nævomatose basocellulaire multiple
n1=en:orofaciodigital syndromes | n2=nævomatose basocellulaire multiple | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
onycho-ostéodysostose
n1=en:orofaciodigital syndromes | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
onycho-patellaire (syndrome)
n1=en:orofaciodigital syndromes | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
parasitologie
n1=en:orofaciodigital syndromes | n2=parasitologie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
phacomatose congenitale
n1=en:orofaciodigital syndromes | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
plagiocéphalie
n1=en:orofaciodigital syndromes | n2=plagiocéphalie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
rubéole congénitale
n1=en:orofaciodigital syndromes | n2=rubéole congénitale | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
Silver-Russell (syndrome de)
n1=en:orofaciodigital syndromes | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
situs inversus
n1=en:orofaciodigital syndromes | n2=situs inversus | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
Sotos (syndrome de)
n1=en:orofaciodigital syndromes | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
Syndrome d'Angelman
n1=en:orofaciodigital syndromes | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome d'Angelman
n1=en:orofaciodigital syndromes | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome d'angelman
n1=en:orofaciodigital syndromes | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de fragilité du chromosome X
n1=en:orofaciodigital syndromes | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de Goltz
n1=en:orofaciodigital syndromes | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de goltz
n1=en:orofaciodigital syndromes | n2=syndrome de goltz | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de Gorlin
n1=en:orofaciodigital syndromes | n2=syndrome de Gorlin | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de gorlin
n1=en:orofaciodigital syndromes | n2=syndrome de gorlin | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de Laurence-Moon
n1=en:orofaciodigital syndromes | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de marfan
n1=en:orofaciodigital syndromes | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de Martin-Bell
n1=en:orofaciodigital syndromes | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de Silver-Russell
n1=en:orofaciodigital syndromes | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de silver-russell
n1=en:orofaciodigital syndromes | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de soto
n1=en:orofaciodigital syndromes | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de Sotos
n1=en:orofaciodigital syndromes | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de sotos
n1=en:orofaciodigital syndromes | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome de Zellweger
n1=en:orofaciodigital syndromes | n2=syndrome de Zellweger | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
syndrome hétérotaxique
n1=en:orofaciodigital syndromes | n2=syndrome hétérotaxique | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
trichothiodystrophie
n1=en:orofaciodigital syndromes | n2=trichothiodystrophie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 20 / 0.465 ->
trisomie
n1=en:orofaciodigital syndromes | n2=trisomie | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndromes --
r_associated #0: 1 / 0.023 ->
en:disease or syndrome
n1=en:orofaciodigital syndromes | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=1
| ≈ 389 relations entrantes
- Goltz ---
r_associated #0: 403 -->
en:orofaciodigital syndromes
n1=Goltz | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=403
- hypoplasie dermique focale ---
r_associated #0: 402 -->
en:orofaciodigital syndromes
n1=hypoplasie dermique focale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=402
- syndrome de Goltz ---
r_associated #0: 402 -->
en:orofaciodigital syndromes
n1=syndrome de Goltz | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=402
- en:focal dermal hypoplasia ---
r_associated #0: 395 -->
en:orofaciodigital syndromes
n1=en:focal dermal hypoplasia | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=395
- hypoplasie dermique en aires ---
r_associated #0: 388 -->
en:orofaciodigital syndromes
n1=hypoplasie dermique en aires | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=388
- en:marfan syndrome ---
r_associated #0: 285 -->
en:orofaciodigital syndromes
n1=en:marfan syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=285
- maladie de Marfan ---
r_associated #0: 281 -->
en:orofaciodigital syndromes
n1=maladie de Marfan | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=281
- syndrome de Marfan ---
r_associated #0: 281 -->
en:orofaciodigital syndromes
n1=syndrome de Marfan | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=281
- en:craniosynostosis ---
r_associated #0: 278 -->
en:orofaciodigital syndromes
n1=en:craniosynostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=278
- crânio-sténose ---
r_associated #0: 277 -->
en:orofaciodigital syndromes
n1=crânio-sténose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=277
- crâniosynostose ---
r_associated #0: 276 -->
en:orofaciodigital syndromes
n1=crâniosynostose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=276
- craniosynostose ---
r_associated #0: 275 -->
en:orofaciodigital syndromes
n1=craniosynostose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=275
- arachnodactylie ---
r_associated #0: 274 -->
en:orofaciodigital syndromes
n1=arachnodactylie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=274
- crâniosténose ---
r_associated #0: 273 -->
en:orofaciodigital syndromes
n1=crâniosténose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=273
- en:arachnodactyly ---
r_associated #0: 253 -->
en:orofaciodigital syndromes
n1=en:arachnodactyly | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=253
- syndrome de soto ---
r_associated #0: 210 -->
en:orofaciodigital syndromes
n1=syndrome de soto | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=210
- en:sotos syndrome ---
r_associated #0: 203 -->
en:orofaciodigital syndromes
n1=en:sotos syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=203
- en:enzymology ---
r_associated #0: 201 -->
en:orofaciodigital syndromes
n1=en:enzymology | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=201
- gigantisme cérébral ---
r_associated #0: 201 -->
en:orofaciodigital syndromes
n1=gigantisme cérébral | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=201
- enzymologie ---
r_associated #0: 200 -->
en:orofaciodigital syndromes
n1=enzymologie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=200
- syndrome de Sotos ---
r_associated #0: 195 -->
en:orofaciodigital syndromes
n1=syndrome de Sotos | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=195
- en:sotos' syndrome ---
r_associated #0: 190 -->
en:orofaciodigital syndromes
n1=en:sotos' syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=190
- craniosténose ---
r_associated #0: 185 -->
en:orofaciodigital syndromes
n1=craniosténose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=185
- en:zellweger syndrome ---
r_associated #0: 169 -->
en:orofaciodigital syndromes
n1=en:zellweger syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=169
- en:Zellweger syndrome ---
r_associated #0: 165 -->
en:orofaciodigital syndromes
n1=en:Zellweger syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=165
- en:parasitology ---
r_associated #0: 162 -->
en:orofaciodigital syndromes
n1=en:parasitology | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=162
- enzymology ---
r_associated #0: 160 -->
en:orofaciodigital syndromes
n1=enzymology | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=160
- parasitologie ---
r_associated #0: 160 -->
en:orofaciodigital syndromes
n1=parasitologie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=160
- en:angelman syndrome ---
r_associated #0: 134 -->
en:orofaciodigital syndromes
n1=en:angelman syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=134
- syndrome d'Angelman ---
r_associated #0: 130 -->
en:orofaciodigital syndromes
n1=syndrome d'Angelman | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=130
- plagiocéphalie ---
r_associated #0: 116 -->
en:orofaciodigital syndromes
n1=plagiocéphalie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=116
- en:plagiocephaly ---
r_associated #0: 112 -->
en:orofaciodigital syndromes
n1=en:plagiocephaly | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=112
- monilethrix ---
r_associated #0: 92 -->
en:orofaciodigital syndromes
n1=monilethrix | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=92
- en:Angelman syndrome ---
r_associated #0: 90 -->
en:orofaciodigital syndromes
n1=en:Angelman syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=90
- en:monilethrix ---
r_associated #0: 90 -->
en:orofaciodigital syndromes
n1=en:monilethrix | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=90
- Syndrome d'Angelman ---
r_associated #0: 70 -->
en:orofaciodigital syndromes
n1=Syndrome d'Angelman | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=70
- syndrome d'angelman ---
r_associated #0: 62 -->
en:orofaciodigital syndromes
n1=syndrome d'angelman | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=62
- en:Sotos' syndrome ---
r_associated #0: 60 -->
en:orofaciodigital syndromes
n1=en:Sotos' syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=60
- situs inversus ---
r_associated #0: 60 -->
en:orofaciodigital syndromes
n1=situs inversus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=60
- syndrome oro-digito-facial ---
r_associated #0: 60 -->
en:orofaciodigital syndromes
n1=syndrome oro-digito-facial | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=60
- syndrome orodigitofacial ---
r_associated #0: 58 -->
en:orofaciodigital syndromes
n1=syndrome orodigitofacial | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=58
- en:situs inversus ---
r_associated #0: 56 -->
en:orofaciodigital syndromes
n1=en:situs inversus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=56
- syndrome de silver-russell ---
r_associated #0: 55 -->
en:orofaciodigital syndromes
n1=syndrome de silver-russell | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=55
- en:down syndrome ---
r_associated #0: 54 -->
en:orofaciodigital syndromes
n1=en:down syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=54
- en:russell-silver syndrome ---
r_associated #0: 54 -->
en:orofaciodigital syndromes
n1=en:russell-silver syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=54
- syndrome de Silver-Russell ---
r_associated #0: 54 -->
en:orofaciodigital syndromes
n1=syndrome de Silver-Russell | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=54
- dysplasie cléidocrânienne ---
r_associated #0: 52 -->
en:orofaciodigital syndromes
n1=dysplasie cléidocrânienne | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=52
- naevomatose baso-cellulaire ---
r_associated #0: 52 -->
en:orofaciodigital syndromes
n1=naevomatose baso-cellulaire | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=52
- syndrome de Gorlin ---
r_associated #0: 51 -->
en:orofaciodigital syndromes
n1=syndrome de Gorlin | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=51
- dysplasie cléido-crânienne ---
r_associated #0: 50 -->
en:orofaciodigital syndromes
n1=dysplasie cléido-crânienne | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=50
- en:Down syndrome ---
r_associated #0: 50 -->
en:orofaciodigital syndromes
n1=en:Down syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=50
- naevomatose basocellulaire ---
r_associated #0: 49 -->
en:orofaciodigital syndromes
n1=naevomatose basocellulaire | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=49
- syndrome hétérotaxique ---
r_associated #0: 49 -->
en:orofaciodigital syndromes
n1=syndrome hétérotaxique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=49
- en:prader-willi syndrome ---
r_associated #0: 48 -->
en:orofaciodigital syndromes
n1=en:prader-willi syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=48
- maladie de marfan ---
r_associated #0: 48 -->
en:orofaciodigital syndromes
n1=maladie de marfan | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=48
- en:Prader-Willi syndrome ---
r_associated #0: 45 -->
en:orofaciodigital syndromes
n1=en:Prader-Willi syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=45
- en:heterotaxy syndrome ---
r_associated #0: 45 -->
en:orofaciodigital syndromes
n1=en:heterotaxy syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=45
- nævomatose basocellulaire multiple ---
r_associated #0: 45 -->
en:orofaciodigital syndromes
n1=nævomatose basocellulaire multiple | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=45
- en:Marfan's syndrome ---
r_associated #0: 44 -->
en:orofaciodigital syndromes
n1=en:Marfan's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=44
- en:situs mutatus ---
r_associated #0: 44 -->
en:orofaciodigital syndromes
n1=en:situs mutatus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=44
- syndrome de goltz ---
r_associated #0: 44 -->
en:orofaciodigital syndromes
n1=syndrome de goltz | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=44
- en:leopard syndrome ---
r_associated #0: 43 -->
en:orofaciodigital syndromes
n1=en:leopard syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=43
- syndrome de marfan ---
r_associated #0: 42 -->
en:orofaciodigital syndromes
n1=syndrome de marfan | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=42
- trichothiodystrophie ---
r_associated #0: 42 -->
en:orofaciodigital syndromes
n1=trichothiodystrophie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=42
- en:nevoid basal cell carcinoma syndrome ---
r_associated #0: 41 -->
en:orofaciodigital syndromes
n1=en:nevoid basal cell carcinoma syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=41
- en:pelviscapular dysplasia ---
r_associated #0: 41 -->
en:orofaciodigital syndromes
n1=en:pelviscapular dysplasia | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=41
- syndrome de sotos ---
r_associated #0: 41 -->
en:orofaciodigital syndromes
n1=syndrome de sotos | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=41
- en:gardner syndrome ---
r_associated #0: 40 -->
en:orofaciodigital syndromes
n1=en:gardner syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=40
- dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- en:orofaciodigital syndrome ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- en:pharmacotherapeutic ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=en:pharmacotherapeutic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- en:trichothiodystrophy ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=en:trichothiodystrophy | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- microbiologique ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=microbiologique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- phacomatose congenitale ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=phacomatose congenitale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- rubéole congénitale ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=rubéole congénitale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- syndrome oro-facio-digital ---
r_associated #0: 39 -->
en:orofaciodigital syndromes
n1=syndrome oro-facio-digital | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=39
- ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) ---
r_associated #0: 38 -->
en:orofaciodigital syndromes
n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=38
- en:basal cell nevus syndrome ---
r_associated #0: 38 -->
en:orofaciodigital syndromes
n1=en:basal cell nevus syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=38
- en:preaxial deficiency, postaxial polydactyly and hypospadias ---
r_associated #0: 38 -->
en:orofaciodigital syndromes
n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=38
- en:situs inversus viscerum ---
r_associated #0: 38 -->
en:orofaciodigital syndromes
n1=en:situs inversus viscerum | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=38
- épidémiologique ---
r_associated #0: 38 -->
en:orofaciodigital syndromes
n1=épidémiologique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=38
- dysostose craniofaciale ---
r_associated #0: 37 -->
en:orofaciodigital syndromes
n1=dysostose craniofaciale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=37
- dystrophie orbitaire congénitale ---
r_associated #0: 37 -->
en:orofaciodigital syndromes
n1=dystrophie orbitaire congénitale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=37
- en:congenital rubella ---
r_associated #0: 37 -->
en:orofaciodigital syndromes
n1=en:congenital rubella | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=37
- en:craniofacial dysostosis ---
r_associated #0: 37 -->
en:orofaciodigital syndromes
n1=en:craniofacial dysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=37
- en:microbiological ---
r_associated #0: 37 -->
en:orofaciodigital syndromes
n1=en:microbiological | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=37
- holoprosencéphalie familiale alobaire de type 1 ---
r_associated #0: 37 -->
en:orofaciodigital syndromes
n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=37
- trisomie ---
r_associated #0: 37 -->
en:orofaciodigital syndromes
n1=trisomie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=37
- dysostose acrofaciale ---
r_associated #0: 36 -->
en:orofaciodigital syndromes
n1=dysostose acrofaciale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=36
- déficit en prolidase ---
r_associated #0: 36 -->
en:orofaciodigital syndromes
n1=déficit en prolidase | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=36
- en:cerebral gigantism ---
r_associated #0: 36 -->
en:orofaciodigital syndromes
n1=en:cerebral gigantism | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=36
- holoprosencéphalie de type 2 ---
r_associated #0: 36 -->
en:orofaciodigital syndromes
n1=holoprosencéphalie de type 2 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=36
- dysostose crânio-faciale ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=dysostose crânio-faciale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- dysplasie ectodermique ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=dysplasie ectodermique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:22q11 deletion syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:22q11 deletion syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:acrofacial dysostosis ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:acrofacial dysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:barth syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:barth syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:beckwith-wiedemann syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:beckwith-wiedemann syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:cockayne syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:cockayne syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:donohue syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:donohue syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:ectodermal dysplasia ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:ectodermal dysplasia | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:epidemiologic ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:epidemiologic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:fragile X syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:fragile X syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:fragile x syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:fragile x syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:heterotaxy ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:heterotaxy | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:holoprosencephaly ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:holoprosencephaly | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:laurence-moon syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:laurence-moon syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:noonan syndrome ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:noonan syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:orofaciodigital syndrome 4 ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 4 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:pentalogy of cantrell ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:pentalogy of cantrell | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:prolidase deficiency ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:prolidase deficiency | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- en:psychology qualifier ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=en:psychology qualifier | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- holoprosencéphalie ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=holoprosencéphalie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- hétérotaxie ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=hétérotaxie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- syndrome de Laurence-Moon ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=syndrome de Laurence-Moon | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- syndrome de fragilité du chromosome X ---
r_associated #0: 35 -->
en:orofaciodigital syndromes
n1=syndrome de fragilité du chromosome X | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=35
- Sotos (syndrome de) ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=Sotos (syndrome de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- dysmorphie des freins buccaux ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=dysmorphie des freins buccaux | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:Marfan's disease ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:Marfan's disease | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:aspects of radionuclide imaging ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:aspects of radionuclide imaging | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:dysostosis ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:dysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:dysostosis of bone of skull ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:dysostosis of bone of skull | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:opitz g/bbb syndrome ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:opitz g/bbb syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:progressive non-infectious anterior vertebral fusion ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:progressive non-infectious anterior vertebral fusion | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:waardenburg syndrome ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=en:waardenburg syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- onycho-patellaire (syndrome) ---
r_associated #0: 34 -->
en:orofaciodigital syndromes
n1=onycho-patellaire (syndrome) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=34
- en:Goltz syndrome ---
r_associated #0: 33 -->
en:orofaciodigital syndromes
n1=en:Goltz syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=33
- en:trisomy ---
r_associated #0: 33 -->
en:orofaciodigital syndromes
n1=en:trisomy | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=33
- holoprosencéphalie de type 4 ---
r_associated #0: 33 -->
en:orofaciodigital syndromes
n1=holoprosencéphalie de type 4 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=33
- onycho-ostéodysostose ---
r_associated #0: 33 -->
en:orofaciodigital syndromes
n1=onycho-ostéodysostose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=33
- dysmorphies des freins buccaux ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=dysmorphies des freins buccaux | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- dysostose crâniofaciale ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=dysostose crâniofaciale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- dysplasie ectodermique, ectrodactylie et dystrophie maculaire ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:Soto's syndrome ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:Soto's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:bardet-biedl syndrome ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:bardet-biedl syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:cleidocranial dysplasia ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:cleidocranial dysplasia | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:isolated noncompaction of the ventricular myocardium ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:isolated noncompaction of the ventricular myocardium | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:ornithine carbamoyltransferase deficiency disease ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:orofaciodigital syndrome 12 ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 12 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:sex chromosome disorders ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:sex chromosome disorders | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:sex chromosome disorders of sex development ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:sex chromosome disorders of sex development | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- en:x chromosome-linked pyridoxine refractory sideroblastic anemia ---
r_associated #0: 32 -->
en:orofaciodigital syndromes
n1=en:x chromosome-linked pyridoxine refractory sideroblastic anemia | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=32
- Silver-Russell (syndrome de) ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=Silver-Russell (syndrome de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- Syndrome de Marfan ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=Syndrome de Marfan | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- dysostoses oro-digito-faciales ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=dysostoses oro-digito-faciales | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:carney complex ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:carney complex | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:complication aspects ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:complication aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:fronto-naso-ethmoidal dysostosis ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:fronto-naso-ethmoidal dysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:genetic diseases, x-linked ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:genetic diseases, x-linked | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:melhem fahl syndrome ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:melhem fahl syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:melnick-fraser syndrome ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:melnick-fraser syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:nail-patella syndrome ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:nail-patella syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- en:spheno-frontal dysostosis ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=en:spheno-frontal dysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- holoprosencéphalie de type 3 ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=holoprosencéphalie de type 3 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- syndrome de Martin-Bell ---
r_associated #0: 31 -->
en:orofaciodigital syndromes
n1=syndrome de Martin-Bell | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
- AFD de type Catania ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=AFD de type Catania | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- Syndrome de Gorlin ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=Syndrome de Gorlin | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- anomalies morphologiques maxillofaciales ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=anomalies morphologiques maxillofaciales | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:charge syndrome ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:charge syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:chemically induced ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:chemically induced | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:cri du chat syndrome ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:cri du chat syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:maxillofacial abnormalities ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:maxillofacial abnormalities | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:netherton syndrome ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:netherton syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:orofaciodigital syndrome 3 ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 3 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:smith-magenis syndrome ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:smith-magenis syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:syndrome, mohr ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=en:syndrome, mohr | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- malformations maxillo-faciales ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=malformations maxillo-faciales | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- malformations maxillofaciales ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=malformations maxillofaciales | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- syndromes oro-facio-digitaux ---
r_associated #0: 30 -->
en:orofaciodigital syndromes
n1=syndromes oro-facio-digitaux | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=30
- en:and mental retardation ---
r_associated #0: 29 -->
en:orofaciodigital syndromes
n1=en:and mental retardation | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=29
- en:craniostenosis ---
r_associated #0: 29 -->
en:orofaciodigital syndromes
n1=en:craniostenosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=29
- en:deaf-blind disorders ---
r_associated #0: 29 -->
en:orofaciodigital syndromes
n1=en:deaf-blind disorders | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=29
- en:ethnologic ---
r_associated #0: 29 -->
en:orofaciodigital syndromes
n1=en:ethnologic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=29
- en:spondylocostal dysostosis ---
r_associated #0: 29 -->
en:orofaciodigital syndromes
n1=en:spondylocostal dysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=29
- en:spondylocostal dysostosis 4, autosomal dominant ---
r_associated #0: 29 -->
en:orofaciodigital syndromes
n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=29
- triskélion ---
r_associated #0: 29 -->
en:orofaciodigital syndromes
n1=triskélion | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=29
- aplasie de la paroi abdominale ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=aplasie de la paroi abdominale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:arachnodactily ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:arachnodactily | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:aspects of mortality statistics ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:aspects of mortality statistics | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:cleft lip and palate ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:cleft lip and palate | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:cleft lip/palate with abnormal thumbs and microcephaly ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:cleft lip/palate with abnormal thumbs and microcephaly | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:mandibuloacral dysplasia with type a lipodystrophy ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:mobius syndrome ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:mobius syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:morava mehes syndrome ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:morava mehes syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:polydactyly, preaxial ii (disorder) ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:polydactyly, preaxial ii (disorder) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- en:wolf-hirschhorn syndrome ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=en:wolf-hirschhorn syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- syndrome de Zellweger ---
r_associated #0: 28 -->
en:orofaciodigital syndromes
n1=syndrome de Zellweger | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=28
- TPN ou NADP ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=TPN ou NADP | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:costello syndrome ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:costello syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:craniofacial abnormalities ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:craniofacial abnormalities | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:etiology aspects ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:etiology aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:ischio-vertebral syndrome ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:ischio-vertebral syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:juvenile x-linked retinoschisis ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:juvenile x-linked retinoschisis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:prune belly syndrome ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:prune belly syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:roentgenographic ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:roentgenographic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- en:therapeutic aspects ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=en:therapeutic aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- syndrome de gorlin ---
r_associated #0: 27 -->
en:orofaciodigital syndromes
n1=syndrome de gorlin | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=27
- chondrodysplasie léthale avec brièveté des côtes ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=chondrodysplasie léthale avec brièveté des côtes | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:Donohue syndrome ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:Donohue syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:acrodysostosis ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:acrodysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:alagille syndrome ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:alagille syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:basal cell nævus ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:basal cell nævus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:marfan's syndrome ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:marfan's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:onychoosteodysostosis ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:onychoosteodysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndrome 13 ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 13 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndrome type 6 ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome type 6 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:orofaciodigital syndrome vii ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome vii | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- en:short rib-polydactyly syndrome ---
r_associated #0: 26 -->
en:orofaciodigital syndromes
n1=en:short rib-polydactyly syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=26
- Goltz (syndrome de) ---
r_associated #0: 25 -->
en:orofaciodigital syndromes
n1=Goltz (syndrome de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=25
- Hölmgren (triade de) ---
r_associated #0: 25 -->
en:orofaciodigital syndromes
n1=Hölmgren (triade de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=25
- en:Gorlin syndrome ---
r_associated #0: 25 -->
en:orofaciodigital syndromes
n1=en:Gorlin syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=25
- en:dysostegenesis ---
r_associated #0: 25 -->
en:orofaciodigital syndromes
n1=en:dysostegenesis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=25
- acrodysostose ---
r_associated #0: 24 -->
en:orofaciodigital syndromes
n1=acrodysostose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=24
- en:Laurence-Moon's syndrome ---
r_associated #0: 24 -->
en:orofaciodigital syndromes
n1=en:Laurence-Moon's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=24
- en:Martin-Bell's syndrome ---
r_associated #0: 24 -->
en:orofaciodigital syndromes
n1=en:Martin-Bell's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=24
- en:hand and foot deformity ---
r_associated #0: 24 -->
en:orofaciodigital syndromes
n1=en:hand and foot deformity | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=24
- ethnologique ---
r_associated #0: 24 -->
en:orofaciodigital syndromes
n1=ethnologique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=24
- maladie du cri du chat ---
r_associated #0: 24 -->
en:orofaciodigital syndromes
n1=maladie du cri du chat | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=24
- dysmorphie orodactyle ---
r_associated #0: 23 -->
en:orofaciodigital syndromes
n1=dysmorphie orodactyle | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=23
- Marfan (maladie de) ---
r_associated #0: 22 -->
en:orofaciodigital syndromes
n1=Marfan (maladie de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=22
- radiographique ---
r_associated #0: 22 -->
en:orofaciodigital syndromes
n1=radiographique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=22
- dysostose ---
r_associated #0: 21 -->
en:orofaciodigital syndromes
n1=dysostose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=21
- en:Angelman's syndrome ---
r_associated #0: 21 -->
en:orofaciodigital syndromes
n1=en:Angelman's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=21
- en:epidemiological ---
r_associated #0: 21 -->
en:orofaciodigital syndromes
n1=en:epidemiological | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=21
- microdélétion 5q35 ---
r_associated #0: 21 -->
en:orofaciodigital syndromes
n1=microdélétion 5q35 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=21
- syndrome de Prader-Willi ---
r_associated #0: 21 -->
en:orofaciodigital syndromes
n1=syndrome de Prader-Willi | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=21
- en:alstrom syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:alstrom syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:bloom syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:bloom syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:congenital abnormal synostosis ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:congenital abnormal synostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:diagnosis aspect ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:diagnosis aspect | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:embryologic ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:embryologic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:exposure as collected domain ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:exposure as collected domain | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:fraser syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:fraser syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:fronto-frontal dysostosis ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:fronto-frontal dysostosis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:genetic aspects ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:genetic aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:historical aspects qualifier ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:historical aspects qualifier | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:immunology aspects ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:immunology aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:in blood ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:in blood | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:in cerebrospinal fluid ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:in cerebrospinal fluid | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:in urine ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:in urine | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:incontinentia pigmenti ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:incontinentia pigmenti | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:klippel-feil syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:klippel-feil syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:loeys-dietz syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:loeys-dietz syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:macrocephaly ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:macrocephaly | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:metabolic aspects ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:metabolic aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:microcephaly ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:microcephaly | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:multiple congenital anomalies ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:multiple congenital anomalies | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:nursing therapy ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:nursing therapy | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:nutritional management ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:nutritional management | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:oculocerebrorenal syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:oculocerebrorenal syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:organoid nevus ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:organoid nevus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 11 ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 11 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 5 ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 5 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 8 ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 8 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 9 ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome 9 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome type 1 ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome type 1 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome x ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:orofaciodigital syndrome x | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:pallister-hall syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:pallister-hall syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:pathological aspects ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:pathological aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:physiopathological ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:physiopathological | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:platybasia ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:platybasia | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:poems syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:poems syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:proteus syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:proteus syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:radiotherapeutic ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:radiotherapeutic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:rehabilitation aspects ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:rehabilitation aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:rubinstein-taybi syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:rubinstein-taybi syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:smith-lemli-opitz syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:smith-lemli-opitz syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:surgical aspects ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:surgical aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:taxonomic ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:taxonomic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:use of ultrasonography ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:use of ultrasonography | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:veterinary aspects ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:veterinary aspects | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:viruses ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:viruses | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- en:weill-marchesani syndrome ---
r_associated #0: 20 -->
en:orofaciodigital syndromes
n1=en:weill-marchesani syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=20
- trisomie 21 ---
r_associated #0: 16 -->
en:orofaciodigital syndromes
n1=trisomie 21 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=16
- Enzymologie ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=Enzymologie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- Giessen (test de) ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=Giessen (test de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- Maladie de Marfan ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=Maladie de Marfan | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- Parasitologie ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=Parasitologie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- goltz ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=goltz | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- triple arthrodèse ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=triple arthrodèse | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- triple opération à la française ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=triple opération à la française | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- triploïdie ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=triploïdie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- triptans ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=triptans | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- triquétrum ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=triquétrum | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- triradialis sulcus de Turner ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=triradialis sulcus de Turner | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- tris ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=tris | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- trismus ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=trismus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- trisomie du bras court du chromosome 3 ---
r_associated #0: 15 -->
en:orofaciodigital syndromes
n1=trisomie du bras court du chromosome 3 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=15
- lepréchaunisme ---
r_associated #0: 11 -->
en:orofaciodigital syndromes
n1=lepréchaunisme | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=11
- mongolisme ---
r_associated #0: 11 -->
en:orofaciodigital syndromes
n1=mongolisme | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=11
- Angelman (syndrome d') ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Angelman (syndrome d') | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Craniosynostose ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Craniosynostose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- DYSOSTOSE ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=DYSOSTOSE | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Gorlin (syndrome de) ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Gorlin (syndrome de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- HLP3 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=HLP3 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- HPE3 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=HPE3 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- HPE4 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=HPE4 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Laurence-Moon (syndrome de) ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Laurence-Moon (syndrome de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Martin-Bell (syndrome de) ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Martin-Bell (syndrome de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Paraquat ® (intoxication par le) ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Paraquat ® (intoxication par le) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Plagiocéphalie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Plagiocéphalie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Ruben (valve de) ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Ruben (valve de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Situs inversus ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Situs inversus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Syndrome de Prader-Willi ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Syndrome de Prader-Willi | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Syndrome de Sotos ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Syndrome de Sotos | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Trichothiodystrophie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Trichothiodystrophie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Trisomie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=Trisomie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectodermitis erosiva pluriorificialis ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectodermitis erosiva pluriorificialis | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectodermose ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectodermose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectodermose érosive pluriorificielle de Fiessinger-Rendu ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectoenzyme ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectoenzyme | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectomie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectomie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectomorphie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectomorphie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectoparasite ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectoparasite | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectoparasitose ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectoparasitose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectopie cardiaque ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectopie cardiaque | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectopie des procès ciliaires ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectopie des procès ciliaires | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- ectopie du cristallin ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=ectopie du cristallin | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:5p minus syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:5p minus syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:5q microdeletion ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:5q microdeletion | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Carney complex ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Carney complex | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Crouzon's disease ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Crouzon's disease | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Crouzon?s disease ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Crouzon?s disease | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Down's ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Down's | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Down's syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Down's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:LEOPARD syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:LEOPARD syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Lejeune's syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Lejeune's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:PWS ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:PWS | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Smith-Magenis syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Smith-Magenis syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:Sotos's syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:Sotos's syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:abdominal wall aplasia ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:abdominal wall aplasia | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:cat cry disease ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:cat cry disease | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:cat cry syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:cat cry syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:chromosome 5p deletion syndrome ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:chromosome 5p deletion syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:ectrodactyly and macular dystrophy ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:ectrodactyly and macular dystrophy | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:ethnological ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:ethnological | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:radiographic ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:radiographic | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:trisomy 21 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:trisomy 21 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:type 1 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:type 1 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:type 2 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:type 2 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:type 3 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:type 3 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- en:type 4 ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=en:type 4 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- fente nasolabiopalatine ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=fente nasolabiopalatine | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holocentromère ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holocentromère | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holocentromérique ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holocentromérique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holocrine ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holocrine | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holodiastolique ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holodiastolique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holoenzyme ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holoenzyme | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- hologamie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=hologamie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- hologynique ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=hologynique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holomérocrine ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holomérocrine | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holophrase ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holophrase | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- holoproencéphalie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=holoproencéphalie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- incontinentia pigmenti ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=incontinentia pigmenti | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- macrocéphalie ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=macrocéphalie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- mongolique (tache) ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=mongolique (tache) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- paraplégie spastique dans la syphilis congénitale ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=paraplégie spastique dans la syphilis congénitale | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- prolidase (déficit en) ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=prolidase (déficit en) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- quadriplégie spastique, rétinite pigmentaire et retard mental ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire et retard mental ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=rétinite pigmentaire et retard mental | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- situs inversus viscerum ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=situs inversus viscerum | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- situs mutatus ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=situs mutatus | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- souche de référence ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=souche de référence | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- souche transduite ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=souche transduite | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- syndrome de zellweger ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=syndrome de zellweger | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- taxinomique ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=taxinomique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- triphosphopyridine-nucléotide ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=triphosphopyridine-nucléotide | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- trisomie 9p ---
r_associated #0: 10 -->
en:orofaciodigital syndromes
n1=trisomie 9p | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=10
- Maladie du cri du chat ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=Maladie du cri du chat | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- Microbiologique ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=Microbiologique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- Onsager (relation d') ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=Onsager (relation d') | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- cri du chat (maladie du) ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=cri du chat (maladie du) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- en:cat's cry syndrome ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=en:cat's cry syndrome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- nævique irien (syndrome) ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=nævique irien (syndrome) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- onychodysplasie ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=onychodysplasie | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- onychogryphose ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=onychogryphose | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- onycholyse ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=onycholyse | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- onycholyse candidosique ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=onycholyse candidosique | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- onycholyse semi-lunaire partielle ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=onycholyse semi-lunaire partielle | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- onychomadèse ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=onychomadèse | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- onychomatricome ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=onychomatricome | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- triplet (CGG) n ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=triplet (CGG) n | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- trisomie 13 ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=trisomie 13 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- trisomie 17p11.2 ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=trisomie 17p11.2 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- trisomie 18 ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=trisomie 18 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
- trisomie 8 ---
r_associated #0: 5 -->
en:orofaciodigital syndromes
n1=trisomie 8 | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=5
|