ZFIN Human Disease: hereditary sensory and autonomic neuropathy type 6

OBO ID: DOID:0070151

Term Name:	hereditary sensory and autonomic neuropathy type 6		Search Ontology:
Synonyms:	hereditary sensory and autonomic neuropathy type VI HSAN6
Definition:	A hereditary sensory neuropathy characterized by neonatal hypotonia, respiratory and feeding difficulties, impaired psychomotor development, and autonomic abnormalities that has_material_basis_in homozygous mutation in the DST gene on chromosome 6p12. https://www.ncbi.nlm.nih.gov/pubmed/22522446
References:	ICD10CM:G60.8 OMIM:614653 ORDO:314381
Ontology:	Human Disease ( DOID:0070151 )

Relationships

is a type of:	autosomal recessive disease hereditary sensory neuropathy autosomal recessive disease hereditary sensory neuropathy Show first 5 Terms

OTHER hereditary sensory and autonomic neuropathy type 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DST	dst	Neuropathy, hereditary sensory and autonomic, type VI	614653

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None