About   Help   FAQ
Disease Ontology Browser
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
05/19/2020
MGI 6.15
The Jackson Laboratory