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Neuropathy, Hereditary Sensory and Autonomic, Type V

^ http://purl.obolibrary.org/obo/NCIT_C156360


An autosomal recessive condition caused by mutation(S) in the NGF gene, encoding beta-nerve growth factor. It is characterized by loss of pain sensation, particularly in the extremities. [ NCI ]

Synonyms: HSAN5, Neuropathy, Hereditary Sensory and Autonomic, Type V

Term info

Preferred Name

Neuropathy, Hereditary Sensory and Autonomic, Type V

Semantic Type

Disease or Syndrome

code

C156360