Agent Commons Collaborative Research
X-linked hereditary sensory and autonomic neuropathy with hearing loss
rareThis syndrome is characterized by the association of an axonal sensory and autonomic neuropathy with hearing loss.
- Identifiers
- MONDO:0010378 OMIM:300614Orphanet:139583
- Causal genes
- AIFM1
- Part of
- X-linked nonsyndromic hearing lossAuditory neuropathyHereditary sensory and autonomic neuropathy
- Also known as
- deafness, X-linked 5 · DFNX5 · X-linked auditory neuropathy with peripheral sensory neuropathy type 1
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