Hearing loss, X-linked 4
- Synonyms
- DEAFNESS, NONSYNDROMIC SENSORINEURAL PROGRESSIVE 6; DEAFNESS, X-LINKED 6, PROGRESSIVE; DFNX4 (DFN6) Nonsyndromic Hearing Loss and Deafness; Deafness, X-linked 4
Summary
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (20 available)
Genes See tests for all associated and related genes
Also known as: Chisel, Csl, DFN6, DFNX4, MPD7, SMPX
Summary: small muscle protein X-linked
Clinical features
Help- Ear malformation
- High-frequency hearing impairment
High-frequency hearing impairment
- MedGen UID: 42358
- Concept ID: C0018780
- Finding: Disease or Syndrome
Ear malformation
- Sensorineural hearing loss disorder
Sensorineural hearing loss disorder
- MedGen UID: 9164
- Concept ID: C0018784
- Finding: Disease or Syndrome
Ear malformation
- High-frequency hearing impairment
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.