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1 OMIM reference -
1 associated gene
17 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
14 signs/symptoms
Craniofacial-deafness-hand syndrome
Hypodontia - dysplasia of nails

PAX3 MSX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PAX3
(0.82)
MSX1



Citations in the biomedical literature:


Craniofacial-deafness-hand syndrome
PAX3
Hypodontia - dysplasia of nails
MSX1



Craniofacial-deafness-hand syndrome
Hypodontia - dysplasia of nails

Synonym(s):
- CDHS
- Sommer-Young-Wee-Frye syndrome

Synonym(s):
- Hypodontia - nail dysgenesis
- Tooth and nail syndrome
- Witkop syndrome

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
- Rare skin disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C536453
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Autosomal dominant inheritance


Craniofacial-deafness-hand syndrome
Hypodontia - dysplasia of nails

Very frequent
- Blepharophimosis / short palpebral fissures
- Defect / anomaly of lacrimal system
- Depressed nasal bridge
- Depressed premaxillary region / midface
- Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures
- Flat face
- Flattened nose
- Hypertelorism
- Microstomia / little mouth
- Narrow face
- Nasal atrophy / hypoplasia / arhinia / rudimentary nose
- Sensorineural deafness / hearing loss
- Short / small nose
- Ulnar deviation of fingers
- Wrist / carpal anomalies

Frequent
- Camptodactyly of some fingers



Very frequent
- Absent / small fingernails / anonychia of hands
- Absent / small toenails / anonychia of feet
- Anodontia / oligodontia / hypodontia
- Anomalies of teeth and dentition
- Delayed dentition / eruption of teeth / lack of eruption of teeth
- Dysplastic / thick / grooved fingernails
- Dysplastic / thick / grooved toenails
- Nails anomalies
- Thin / hypoplastic toenails
- Tooth shape anomaly

Frequent
- Everted lower lip
- Fine hair

Occasional
- Abnormal / polycystic ovaries