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DO Term : autosomal dominant nonsyndromic deafness 36 [DOID:0110563] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.
  • synonyms:
  • OMIM:606705,
  • DFNA36,
  • autosomal dominant deafness 36,
  • 606705,
  • ICD10CM:H90.3
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Disease

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Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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