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Disease Ontology Browser
hereditary sensory and autonomic neuropathy type 2D (DOID:0070689)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type IID; HSAN2D
Alt IDs: UMLS_CUI:C4012054
Definition: A hereditary sensory and autonomic neuropathy type 2 characterized by congenital to pediatric onset of distal loss of pain and temperature sensation and variable autonomic dysfunction that has_material_basis_in homozygous loss-of-function mutation in the SCN9A gene on chromosome 2q24.

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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Send questions and comments to User Support. 		last database update
04/07/2026
MGI 6.24 		The Jackson Laboratory