'en:osteogenesis imperfecta, type xii'
(id=6804387 ; fe=en:osteogenesis imperfecta, type xii ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=2944 creation date=2017-06-25 touchdate=2025-11-02 20:33:28.000) ≈ 49 relations sortantes
- en:osteogenesis imperfecta, type xii --
r_associated #0: 41 / 1 ->
en:no dentinogenesis imperfecta
n1=en:osteogenesis imperfecta, type xii | n2=en:no dentinogenesis imperfecta | rel=r_associated | relid=0 | w=41
- en:osteogenesis imperfecta, type xii --
r_associated #0: 37 / 0.902 ->
en:micrognathism
n1=en:osteogenesis imperfecta, type xii | n2=en:micrognathism | rel=r_associated | relid=0 | w=37
- en:osteogenesis imperfecta, type xii --
r_associated #0: 37 / 0.902 ->
en:osteoporosis
n1=en:osteogenesis imperfecta, type xii | n2=en:osteoporosis | rel=r_associated | relid=0 | w=37
- en:osteogenesis imperfecta, type xii --
r_associated #0: 35 / 0.854 ->
en:autosomal recessive inheritance
n1=en:osteogenesis imperfecta, type xii | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=35
- en:osteogenesis imperfecta, type xii --
r_associated #0: 35 / 0.854 ->
en:hearing normal
n1=en:osteogenesis imperfecta, type xii | n2=en:hearing normal | rel=r_associated | relid=0 | w=35
- en:osteogenesis imperfecta, type xii --
r_associated #0: 35 / 0.854 ->
en:short stature
n1=en:osteogenesis imperfecta, type xii | n2=en:short stature | rel=r_associated | relid=0 | w=35
- en:osteogenesis imperfecta, type xii --
r_associated #0: 34 / 0.829 ->
en:bowing of upper limb
n1=en:osteogenesis imperfecta, type xii | n2=en:bowing of upper limb | rel=r_associated | relid=0 | w=34
- en:osteogenesis imperfecta, type xii --
r_associated #0: 34 / 0.829 ->
en:high, prominent forehead
n1=en:osteogenesis imperfecta, type xii | n2=en:high, prominent forehead | rel=r_associated | relid=0 | w=34
- en:osteogenesis imperfecta, type xii --
r_associated #0: 32 / 0.78 ->
en:mild bone deformities
n1=en:osteogenesis imperfecta, type xii | n2=en:mild bone deformities | rel=r_associated | relid=0 | w=32
- en:osteogenesis imperfecta, type xii --
r_associated #0: 32 / 0.78 ->
en:mild facial asymmetry
n1=en:osteogenesis imperfecta, type xii | n2=en:mild facial asymmetry | rel=r_associated | relid=0 | w=32
- en:osteogenesis imperfecta, type xii --
r_associated #0: 31 / 0.756 ->
en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001)
n1=en:osteogenesis imperfecta, type xii | n2=en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001) | rel=r_associated | relid=0 | w=31
- en:osteogenesis imperfecta, type xii --
r_associated #0: 30 / 0.732 ->
en:byzanthine arch palate
n1=en:osteogenesis imperfecta, type xii | n2=en:byzanthine arch palate | rel=r_associated | relid=0 | w=30
- en:osteogenesis imperfecta, type xii --
r_associated #0: 30 / 0.732 ->
en:hyperextensibility of the interphalangeal joints
n1=en:osteogenesis imperfecta, type xii | n2=en:hyperextensibility of the interphalangeal joints | rel=r_associated | relid=0 | w=30
- en:osteogenesis imperfecta, type xii --
r_associated #0: 30 / 0.732 ->
en:pectus carinatum
n1=en:osteogenesis imperfecta, type xii | n2=en:pectus carinatum | rel=r_associated | relid=0 | w=30
- en:osteogenesis imperfecta, type xii --
r_associated #0: 30 / 0.732 ->
en:repeated bone fractures
n1=en:osteogenesis imperfecta, type xii | n2=en:repeated bone fractures | rel=r_associated | relid=0 | w=30
- en:osteogenesis imperfecta, type xii --
r_associated #0: 29 / 0.707 ->
en:depressed nasal bridge
n1=en:osteogenesis imperfecta, type xii | n2=en:depressed nasal bridge | rel=r_associated | relid=0 | w=29
- en:osteogenesis imperfecta, type xii --
r_associated #0: 29 / 0.707 ->
en:genu varum
n1=en:osteogenesis imperfecta, type xii | n2=en:genu varum | rel=r_associated | relid=0 | w=29
- en:osteogenesis imperfecta, type xii --
r_associated #0: 29 / 0.707 ->
en:late tooth eruption
n1=en:osteogenesis imperfecta, type xii | n2=en:late tooth eruption | rel=r_associated | relid=0 | w=29
- en:osteogenesis imperfecta, type xii --
r_associated #0: 29 / 0.707 ->
en:microstomia
n1=en:osteogenesis imperfecta, type xii | n2=en:microstomia | rel=r_associated | relid=0 | w=29
- en:osteogenesis imperfecta, type xii --
r_associated #0: 29 / 0.707 ->
en:normal sclerae
n1=en:osteogenesis imperfecta, type xii | n2=en:normal sclerae | rel=r_associated | relid=0 | w=29
- en:osteogenesis imperfecta, type xii --
r_associated #0: 29 / 0.707 ->
en:prominent supraorbital ridges
n1=en:osteogenesis imperfecta, type xii | n2=en:prominent supraorbital ridges | rel=r_associated | relid=0 | w=29
- en:osteogenesis imperfecta, type xii --
r_associated #0: 28 / 0.683 ->
en:hypoplasia of midface
n1=en:osteogenesis imperfecta, type xii | n2=en:hypoplasia of midface | rel=r_associated | relid=0 | w=28
- en:osteogenesis imperfecta, type xii --
r_associated #0: 28 / 0.683 ->
en:mild scoliosis
n1=en:osteogenesis imperfecta, type xii | n2=en:mild scoliosis | rel=r_associated | relid=0 | w=28
- en:osteogenesis imperfecta, type xii --
r_associated #0: 28 / 0.683 ->
en:motor developmental delay
n1=en:osteogenesis imperfecta, type xii | n2=en:motor developmental delay | rel=r_associated | relid=0 | w=28
- en:osteogenesis imperfecta, type xii --
r_associated #0: 28 / 0.683 ->
en:structure of wormian bone
n1=en:osteogenesis imperfecta, type xii | n2=en:structure of wormian bone | rel=r_associated | relid=0 | w=28
- en:osteogenesis imperfecta, type xii --
r_associated #0: 25 / 0.61 ->
en:osteogenesis
n1=en:osteogenesis imperfecta, type xii | n2=en:osteogenesis | rel=r_associated | relid=0 | w=25
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
bébé bronzé (syndrome du)
n1=en:osteogenesis imperfecta, type xii | n2=bébé bronzé (syndrome du) | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
Bec de lièvre
n1=en:osteogenesis imperfecta, type xii | n2=Bec de lièvre | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
bec de lièvre
n1=en:osteogenesis imperfecta, type xii | n2=bec de lièvre | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:and hypogonadotropic hypogonadism
n1=en:osteogenesis imperfecta, type xii | n2=en:and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:and teething delay
n1=en:osteogenesis imperfecta, type xii | n2=en:and teething delay | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:brittle-bone disease
n1=en:osteogenesis imperfecta, type xii | n2=en:brittle-bone disease | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:cleft lip
n1=en:osteogenesis imperfecta, type xii | n2=en:cleft lip | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:cleft palate
n1=en:osteogenesis imperfecta, type xii | n2=en:cleft palate | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:harelip
n1=en:osteogenesis imperfecta, type xii | n2=en:harelip | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:hernia
n1=en:osteogenesis imperfecta, type xii | n2=en:hernia | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:keratoconus posticus
n1=en:osteogenesis imperfecta, type xii | n2=en:keratoconus posticus | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
en:micrognathia
n1=en:osteogenesis imperfecta, type xii | n2=en:micrognathia | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
Fenn (diagramme de)
n1=en:osteogenesis imperfecta, type xii | n2=Fenn (diagramme de) | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
fente labiale
n1=en:osteogenesis imperfecta, type xii | n2=fente labiale | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
fente labiopalatine et blépharophimosis
n1=en:osteogenesis imperfecta, type xii | n2=fente labiopalatine et blépharophimosis | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
hérédité autosomale récessive
n1=en:osteogenesis imperfecta, type xii | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
kératocône postérieur-fente labiale-petite taille
n1=en:osteogenesis imperfecta, type xii | n2=kératocône postérieur-fente labiale-petite taille | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
micrognathie
n1=en:osteogenesis imperfecta, type xii | n2=micrognathie | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
micrognathisme
n1=en:osteogenesis imperfecta, type xii | n2=micrognathisme | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique
n1=en:osteogenesis imperfecta, type xii | n2=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
ostéoporose
n1=en:osteogenesis imperfecta, type xii | n2=ostéoporose | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 20 / 0.488 ->
petite taille, hyperextensibilité, hernie et dépression oculaire
n1=en:osteogenesis imperfecta, type xii | n2=petite taille, hyperextensibilité, hernie et dépression oculaire | rel=r_associated | relid=0 | w=20
- en:osteogenesis imperfecta, type xii --
r_associated #0: 2 / 0.049 ->
en:disease or syndrome
n1=en:osteogenesis imperfecta, type xii | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=2
| ≈ 93 relations entrantes
- micrognathie ---
r_associated #0: 302 -->
en:osteogenesis imperfecta, type xii
n1=micrognathie | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=302
- micrognathisme ---
r_associated #0: 302 -->
en:osteogenesis imperfecta, type xii
n1=micrognathisme | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=302
- en:micrognathism ---
r_associated #0: 300 -->
en:osteogenesis imperfecta, type xii
n1=en:micrognathism | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=300
- kératocône postérieur-fente labiale-petite taille ---
r_associated #0: 50 -->
en:osteogenesis imperfecta, type xii
n1=kératocône postérieur-fente labiale-petite taille | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=50
- en:keratoconus posticus ---
r_associated #0: 46 -->
en:osteogenesis imperfecta, type xii
n1=en:keratoconus posticus | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=46
- en:cleft lip ---
r_associated #0: 45 -->
en:osteogenesis imperfecta, type xii
n1=en:cleft lip | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=45
- bec de lièvre ---
r_associated #0: 44 -->
en:osteogenesis imperfecta, type xii
n1=bec de lièvre | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=44
- en:short stature ---
r_associated #0: 44 -->
en:osteogenesis imperfecta, type xii
n1=en:short stature | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=44
- myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique ---
r_associated #0: 44 -->
en:osteogenesis imperfecta, type xii
n1=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=44
- hérédité autosomale récessive ---
r_associated #0: 41 -->
en:osteogenesis imperfecta, type xii
n1=hérédité autosomale récessive | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=41
- en:harelip ---
r_associated #0: 40 -->
en:osteogenesis imperfecta, type xii
n1=en:harelip | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=40
- fente labiale ---
r_associated #0: 40 -->
en:osteogenesis imperfecta, type xii
n1=fente labiale | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=40
- fente labiopalatine et blépharophimosis ---
r_associated #0: 40 -->
en:osteogenesis imperfecta, type xii
n1=fente labiopalatine et blépharophimosis | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=40
- Fenn (diagramme de) ---
r_associated #0: 38 -->
en:osteogenesis imperfecta, type xii
n1=Fenn (diagramme de) | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=38
- en:autosomal recessive inheritance ---
r_associated #0: 38 -->
en:osteogenesis imperfecta, type xii
n1=en:autosomal recessive inheritance | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=38
- petite taille, hyperextensibilité, hernie et dépression oculaire ---
r_associated #0: 37 -->
en:osteogenesis imperfecta, type xii
n1=petite taille, hyperextensibilité, hernie et dépression oculaire | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=37
- en:depressed nasal bridge ---
r_associated #0: 35 -->
en:osteogenesis imperfecta, type xii
n1=en:depressed nasal bridge | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=35
- en:normal sclerae ---
r_associated #0: 35 -->
en:osteogenesis imperfecta, type xii
n1=en:normal sclerae | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=35
- en:structure of wormian bone ---
r_associated #0: 34 -->
en:osteogenesis imperfecta, type xii
n1=en:structure of wormian bone | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=34
- Bec de lièvre ---
r_associated #0: 33 -->
en:osteogenesis imperfecta, type xii
n1=Bec de lièvre | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=33
- en:high, prominent forehead ---
r_associated #0: 32 -->
en:osteogenesis imperfecta, type xii
n1=en:high, prominent forehead | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=32
- en:micrognathia ---
r_associated #0: 32 -->
en:osteogenesis imperfecta, type xii
n1=en:micrognathia | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=32
- en:prominent supraorbital ridges ---
r_associated #0: 32 -->
en:osteogenesis imperfecta, type xii
n1=en:prominent supraorbital ridges | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=32
- en:and hypogonadotropic hypogonadism ---
r_associated #0: 30 -->
en:osteogenesis imperfecta, type xii
n1=en:and hypogonadotropic hypogonadism | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=30
- en:and teething delay ---
r_associated #0: 30 -->
en:osteogenesis imperfecta, type xii
n1=en:and teething delay | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=30
- en:byzanthine arch palate ---
r_associated #0: 30 -->
en:osteogenesis imperfecta, type xii
n1=en:byzanthine arch palate | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=30
- en:mild bone deformities ---
r_associated #0: 30 -->
en:osteogenesis imperfecta, type xii
n1=en:mild bone deformities | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=30
- en:mild scoliosis ---
r_associated #0: 30 -->
en:osteogenesis imperfecta, type xii
n1=en:mild scoliosis | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=30
- en:cleft palate ---
r_associated #0: 29 -->
en:osteogenesis imperfecta, type xii
n1=en:cleft palate | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=29
- en:hernia ---
r_associated #0: 29 -->
en:osteogenesis imperfecta, type xii
n1=en:hernia | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=29
- en:late tooth eruption ---
r_associated #0: 29 -->
en:osteogenesis imperfecta, type xii
n1=en:late tooth eruption | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=29
- bébé bronzé (syndrome du) ---
r_associated #0: 28 -->
en:osteogenesis imperfecta, type xii
n1=bébé bronzé (syndrome du) | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=28
- en:brittle-bone disease ---
r_associated #0: 28 -->
en:osteogenesis imperfecta, type xii
n1=en:brittle-bone disease | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=28
- en:genu varum ---
r_associated #0: 28 -->
en:osteogenesis imperfecta, type xii
n1=en:genu varum | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=28
- en:hearing normal ---
r_associated #0: 28 -->
en:osteogenesis imperfecta, type xii
n1=en:hearing normal | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=28
- en:no dentinogenesis imperfecta ---
r_associated #0: 28 -->
en:osteogenesis imperfecta, type xii
n1=en:no dentinogenesis imperfecta | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=28
- en:microstomia ---
r_associated #0: 27 -->
en:osteogenesis imperfecta, type xii
n1=en:microstomia | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=27
- en:motor developmental delay ---
r_associated #0: 27 -->
en:osteogenesis imperfecta, type xii
n1=en:motor developmental delay | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=27
- en:osteoporosis ---
r_associated #0: 27 -->
en:osteogenesis imperfecta, type xii
n1=en:osteoporosis | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=27
- en:repeated bone fractures ---
r_associated #0: 27 -->
en:osteogenesis imperfecta, type xii
n1=en:repeated bone fractures | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=27
- ostéoporose ---
r_associated #0: 27 -->
en:osteogenesis imperfecta, type xii
n1=ostéoporose | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=27
- en:labial fissure ---
r_associated #0: 25 -->
en:osteogenesis imperfecta, type xii
n1=en:labial fissure | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=25
- en:mild facial asymmetry ---
r_associated #0: 25 -->
en:osteogenesis imperfecta, type xii
n1=en:mild facial asymmetry | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=25
- en:pectus carinatum ---
r_associated #0: 25 -->
en:osteogenesis imperfecta, type xii
n1=en:pectus carinatum | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=25
- kératocône posticus ---
r_associated #0: 25 -->
en:osteogenesis imperfecta, type xii
n1=kératocône posticus | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=25
- en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001) ---
r_associated #0: 24 -->
en:osteogenesis imperfecta, type xii
n1=en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001) | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=24
- en:multicore disease with mental retardation ---
r_associated #0: 24 -->
en:osteogenesis imperfecta, type xii
n1=en:multicore disease with mental retardation | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=24
- en:palate-blepharophimosis ---
r_associated #0: 23 -->
en:osteogenesis imperfecta, type xii
n1=en:palate-blepharophimosis | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=23
- en:Rieger anomaly ---
r_associated #0: 22 -->
en:osteogenesis imperfecta, type xii
n1=en:Rieger anomaly | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=22
- en:hyperextensibility ---
r_associated #0: 22 -->
en:osteogenesis imperfecta, type xii
n1=en:hyperextensibility | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=22
- en:ocular depression ---
r_associated #0: 22 -->
en:osteogenesis imperfecta, type xii
n1=en:ocular depression | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=22
- en:bowing of upper limb ---
r_associated #0: 21 -->
en:osteogenesis imperfecta, type xii
n1=en:bowing of upper limb | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=21
- en:hyperextensibility of the interphalangeal joints ---
r_associated #0: 21 -->
en:osteogenesis imperfecta, type xii
n1=en:hyperextensibility of the interphalangeal joints | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=21
- en:hypoplasia of midface ---
r_associated #0: 21 -->
en:osteogenesis imperfecta, type xii
n1=en:hypoplasia of midface | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=21
- insuffisance staturale ---
r_associated #0: 21 -->
en:osteogenesis imperfecta, type xii
n1=insuffisance staturale | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=21
- Fente labiale ---
r_associated #0: 15 -->
en:osteogenesis imperfecta, type xii
n1=Fente labiale | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=15
- fente labio-palatine ---
r_associated #0: 15 -->
en:osteogenesis imperfecta, type xii
n1=fente labio-palatine | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=15
- fente labiopalatine ---
r_associated #0: 15 -->
en:osteogenesis imperfecta, type xii
n1=fente labiopalatine | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=15
- BEC DE LIEVRE ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=BEC DE LIEVRE | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- Micrognathie ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=Micrognathie | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- Ostéoporose ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=Ostéoporose | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- bec de corbin ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=bec de corbin | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- bec de cuiller ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=bec de cuiller | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- bec de la prostate ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=bec de la prostate | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- bec de la rotule ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=bec de la rotule | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- bébé collodion ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=bébé collodion | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- division palatine ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=division palatine | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- en:Fenn's diagram ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=en:Fenn's diagram | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- en:bronze baby syndrome ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=en:bronze baby syndrome | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- en:labiopalatine cleft ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=en:labiopalatine cleft | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente cérébrale de Bichat ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente cérébrale de Bichat | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente de Larrey ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente de Larrey | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente de la glotte ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente de la glotte | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente foetale ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente foetale | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente hypophysaire ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente hypophysaire | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente interaryténoïdienne ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente interaryténoïdienne | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente interfessière ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente interfessière | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente labiopalatine et kystes muqueux de la lèvre inférieure ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente labiopalatine et kystes muqueux de la lèvre inférieure | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente labiopalatine, ectropion et dents coniques ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente labiopalatine, ectropion et dents coniques | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fente palatine ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fente palatine | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fissure palatine ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fissure palatine | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- fénotérol ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=fénotérol | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- genu varum ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=genu varum | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- maladie des os de verre ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=maladie des os de verre | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- micrognatisme ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=micrognatisme | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- microgéodes phalangiennes (syndrome des) ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=microgéodes phalangiennes (syndrome des) | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- pectus carinatum ---
r_associated #0: 10 -->
en:osteogenesis imperfecta, type xii
n1=pectus carinatum | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=10
- bec de perroquet ---
r_associated #0: 5 -->
en:osteogenesis imperfecta, type xii
n1=bec de perroquet | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=5
- bec du cuboïde ---
r_associated #0: 5 -->
en:osteogenesis imperfecta, type xii
n1=bec du cuboïde | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=5
- bec du sphénoïde ---
r_associated #0: 5 -->
en:osteogenesis imperfecta, type xii
n1=bec du sphénoïde | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=5
- bec scléral ---
r_associated #0: 5 -->
en:osteogenesis imperfecta, type xii
n1=bec scléral | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=5
- bécégite ---
r_associated #0: 5 -->
en:osteogenesis imperfecta, type xii
n1=bécégite | n2=en:osteogenesis imperfecta, type xii | rel=r_associated | relid=0 | w=5
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