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Deafness, autosomal recessive 12, modifier of

MedGen UID:: 864325
•Concept ID:: C4015888
•: Finding

Synonym:	DEAFNESS, AUTOSOMAL RECESSIVE 12, MODIFIER OF

OMIM®:	108733

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVHereditary hearing loss and deafness

Hereditary hearing loss and deafness
- Nonsyndromic genetic hearing loss
  - Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive
    - Deafness, autosomal recessive 12, modifier of

Supplemental Content

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Genetic Testing Registry

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ClinicalTrials.gov

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MedlinePlus

Reviews

Related information

ClinVar
Related medical variations
GTR
Related information in GTR
GTR(Clinical)
Clinical tests in GTR
OMIM
Related records in OMIM
PubMed (OMIM)
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