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Echinobase
Summary Literature (0)
DOID:0070157 - hereditary sensory and autonomic neuropathy type 1C

Disease Ontology Definition:A hereditary sensory and autonomic neuropathy type 1 that has_material_basis_in heterozygous mutation in the SPTLC2 gene on chromosome 14q24.

Synonyms: HSAN1C, hereditary sensory and autonomic neuropathy type IC,

Echinobase Genes :


OMIM:
MIM:613640 - neuropathy, hereditary sensory and autonomic, type ic; hsan1c

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), hereditary sensory and autonomic neuropathy type 1 (is_a)