Deafness, Autosomal Dominant 69 (DFNA69)

Alias:

Dcua

Deafness, Autosomal Dominant 69, Unilateral or Asymmetric

Deafness, Congenital, Unilateral or Asymmetric

Autosomal Dominant Nonsyndromic Deafness 69

Dfna69

Autosomal Dominant Nonsyndromic Hearing Loss 69

Unilateral or Asymmetric Congenital Deafness

Autosomal Dominant Deafness 69

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 69, also known as dcua, is related to extracutaneous mastocytoma and solitary mastocytoma of the skin. An important gene associated with Deafness, Autosomal Dominant 69 is KITLG (KIT Ligand), and among its related pathways/superpathways are Tyrosine Kinases / Adaptors and Development EPO-induced Jak-STAT pathway. Affiliated tissues include skin, and related phenotypes are sensorineural hearing impairment and neoplasm

Related ID：

MALACARDS：DFN360

OMIM：616697

MESH：D006319