ODCs

Click node...

4 OMIM references -
4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Hereditary sensory and autonomic neuropathy type 1

Tangier disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SPTLC1	(0.65)	ABCA1

Citations in the biomedical literature:

Hereditary sensory and autonomic neuropathy type 1		Tangier disease
	Synonym(s): (no synonyms)		Synonym(s): - Defective adenosine triphosphate-binding cassette transporter A1

	Classification (Orphanet): - Inborn errors of metabolism - 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): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		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: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D013631

No signs/symptoms info available.