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Disease Ontology Browser
congenital insensitivity to pain with anhidrosis (DOID:0070146)
Alliance: disease page
Synonyms: CIPA; familial dysautonomia type II; hereditary sensory and autonomic neuropathy type 4; hereditary sensory and autonomic neuropathy type IV; hereditary sensory neuropathy type 4; hereditary sensory neuropathy type IV; HSAN4; insensitivity to pain, congenital, with anhidrosis; type II familial dysautonomia
Alt IDs: OMIM:256800, NCI:C118633, ORDO:642, UMLS_CUI:C0020074
Definition: A hereditary sensory and autonomic 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.

Disease References using Mouse Models (3)
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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03/31/2026
MGI 6.24 		The Jackson Laboratory