Disease

autosomal dominant nonsyndromic deafness 69

Name: autosomal dominant nonsyndromic deafness 69
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110590 autosomal dominant nonsyndromic deafness 69 An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21. DCUA DFNA69 autosomal dominant deafness 69 unilateral or asymmetric congenital deafness

Definition

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.

Synonyms

autosomal dominant deafness 69
DCUA

Cross References

ICD10CM:H90.3
MIM:616697

Parent Terms

autosomal dominant nonsyndromic deafness

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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