hearing loss, X-linked 4
MONDO:0010238Mondo
Findings
No curated finding names hearing loss, X-linked 4 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any X-linked nonsyndromic deafness in which the cause of the disease is a mutation in the SMPX gene.
Definition from the Mondo Disease Ontology (MONDO:0010238), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- SMPXHGNC:11122
- Strong · Labcorp Genetics (formerly Invitae) · X-linked · 2021
- Strong · PanelApp Australia · X-linked · 2025
Where it sits
- A kind of