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hereditary sensory and autonomic neuropathy type 7 (DOID:0070149)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type VII; HSAN7
Alt IDs: OMIM:615548, ICD10CM:G60.8, ORDO:391397
Definition: A hereditary sensory neuropathy characterized by insensitivity to pain, mild muscle weakness, delayed motor development, hyperhidrosis and gastrointestinal dysfunction that has_material_basis_in heterozygous mutation in the SCN11A gene on chromosome 3p22.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory