ODCs

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2 OMIM references -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Congenital hereditary facial paralysis with variable hearing loss

Autosomal dominant keratitis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HOXB1	(0.75)	PAX6

Citations in the biomedical literature:

Congenital hereditary facial paralysis with variable hearing loss		Autosomal dominant keratitis
	Synonym(s): - Congenital hereditary facial palsy with variable deafness - Congenital hereditary facial palsy with variable hearing loss - Congenital hereditary facial paralysis with variable deafness		Synonym(s): - Hereditary keratitis

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare neurologic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available 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: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537022

No signs/symptoms info available.