ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Hydranencephaly

Bilateral microtia - deafness - cleft palate


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NDE1	(0.63)	HOXA2

Citations in the biomedical literature:

Hydranencephaly		Bilateral microtia - deafness - cleft palate

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

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

	External references: No OMIM references 1 MeSH reference: D006832		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.