Term Name:	hereditary sensory and autonomic neuropathy type 2
Synonyms:	hereditary sensory and autonomic neuropathy type II, hereditary sensory neuropathy type 2, hereditary sensory neuropathy type II, HSAN2, HSN2
Definition:	A hereditary sensory and autonomic neuropathy characterized by progressive, primarily distal reduced sensation to pain, temperature, and touch with congenital to juvenile onset, autosomal recessive inheritance, and variable, limited autonomic and muscular dysfunction. Loss of sensation commonly results in Charcot joints, unnoticed lacerations, acral mutilations, and osteomyelitis.
Ontology:	Human Disease [DOID:0070161] ( DOID:0070161 )

Relationships

is a type of:	autosomal recessive disease hereditary sensory and autonomic neuropathy
has subtype:	hereditary sensory and autonomic neuropathy type 2A hereditary sensory and autonomic neuropathy type 2B hereditary sensory and autonomic neuropathy type 2D hereditary sensory neuropathy type 2C