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Disease Ontology Browser
hereditary sensory neuropathy type 4 (DOID:0070146)
Alliance: disease page
Synonyms: hereditary sensory neuropathy type IV; insensitivity to pain, congenital, with anhidrosis
Alt IDs: OMIM:256800, MESH:D009477, NCI:C118633, ORDO:642, UMLS_CUI:C0020074
Definition: A hereditary sensory neuropathy characterized by insensitivity to pain and anhidrosis that has_material_basis_in homozygous or compound heterozygous mutation in the NTRK1 gene on chromosome 1q23.


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)
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last database update
07/16/2019
MGI 6.14
The Jackson Laboratory