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DOID:0070154 - hereditary sensory neuropathy type 1F
Disease Ontology Definition:A hereditary sensory and autonomic neuropathy type 1 characterized by sensory loss in the lower limbs developing in the second or third decade of life but absence of autonomic involvement that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13.
Synonyms: HSN1F, hereditary sensory neuropathy type IF,
Echinobase Genes :
MIM:615632 - neuropathy, hereditary sensory, type if; hsn1f |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee