C180844Level 5
X-Linked Deafness-4
**Semantic type:** Disease or Syndrome
**Definition:** An X-linked dominant condition caused by mutation (s) in the SMPX gene, encoding small muscular protein. It is characterized by progressive sensorineural hearing loss.
**Synonyms:** - DFNX4
GET
/api/v1/systems/nci_thesaurus/nodes/C180844Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.