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

Congenital communicating hydrocephalus

Tangier disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MPDZ	(0.65)	ABCA1

Citations in the biomedical literature:

Congenital communicating hydrocephalus		Tangier disease
	Synonym(s): - Congenital non-obstructive hydrocephalus		Synonym(s): - Defective adenosine triphosphate-binding cassette transporter A1

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare endocrine disease - Rare eye disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D013631

No signs/symptoms info available.