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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/09/2019
MGI 6.13
The Jackson Laboratory