hereditary sensory and autonomic neuropathy type 5 (MONDO_0012092, a Monarch Disease Ontology entry) can be described as follows. Hereditary sensory and autonomic neuropathy, type 5 (HSAN5) is characterized by loss of pain perception and impaired temperature sensitivity, in the absence of any other major neurological anomalies. Also known as: HSAN5, NGF autosomal recessive hereditary sensory and autonomic neuropathy, autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF, congenital insensitivity to pain and thermal analgesia, hereditary sensory and autonomic neuropathy type V.