ZFIN Human Disease: hereditary sensory neuropathy type 1D

OBO ID: DOID:0070156

Term Name:	hereditary sensory neuropathy type 1D		Search Ontology:
Synonyms:	HSN1D
Definition:	A hereditary sensory and autonomic neuropathy type 1 characterized dult onset of a distal axonal sensory neuropathy affecting all modalities, often associated with distal ulceration and amputation as well as hyporeflexia, although some patients may show features suggesting upper neuron involvement that has_material_basis_in heterozygous mutation in the ATL1 gene on chromosome 14q. https://www.ncbi.nlm.nih.gov/pubmed/21194679
References:	OMIM:613708
Ontology:	Human Disease ( DOID:0070156 )

Relationships

is a type of:	autosomal dominant disease hereditary sensory and autonomic neuropathy type 1 autosomal dominant disease hereditary sensory and autonomic neuropathy type 1 Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ATL1	atl1	Neuropathy, hereditary sensory, type ID	613708

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None