ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

Oculootodental syndrome

Camptodactyly - tall stature - scoliosis - hearing loss

FADD	(UniProt - OMIM)		FGFR3	(UniProt - OMIM)
FGF3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FGF3	(0.52)	FGFR3

Citations in the biomedical literature:

Oculootodental syndrome		Camptodactyly - tall stature - scoliosis - hearing loss
	Synonym(s): - OOD		Synonym(s): - CATSHL syndrome

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

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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

Camptodactyly - tall stature - scoliosis - hearing loss
	Very frequent - Camptodactyly of fingers - Hearing loss / hypoacusia / deafness - Scoliosis - Tall stature / gigantism / growth acceleration
Oculootodental syndrome
(no data available)