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Date: Tue Jan 28 2025
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autosomal recessive nonsyndromic deafness 1B
DOID:0110476
Summary
Associated Genes
Associated Alleles
Associated Models
Disease
autosomal recessive nonsyndromic deafness 1B
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.
[1]
Synonyms
autosomal recessive deafness 1B
DFNB1B
Cross References
ICD10CM:H90.3
MIM:612645
Parent Terms
autosomal recessive nonsyndromic deafness
Child Terms
None
Sources of Associations
RGD
MGI
ZFIN
FB
WB
SGD
Associated Genes
Associated Alleles
Associated Models
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