ZFIN Human Disease: hereditary sensory neuropathy type 1F

OBO ID: DOID:0070154

Term Name:	hereditary sensory neuropathy type 1F		Search Ontology:
Synonyms:	hereditary sensory neuropathy type IF HSN1F
Definition:	A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/24459106
References:	OMIM:615632
Ontology:	Human Disease ( DOID:0070154 )

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

OTHER hereditary sensory neuropathy type 1F PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ATL3	atl3	Neuropathy, hereditary sensory, type IF	615632

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None