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DO Term : autosomal recessive nonsyndromic deafness 39 [DOID:0110497] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.
  • synonyms:
  • 608265,
  • OMIM:608265,
  • autosomal recessive deafness 39,
  • DFNB39,
  • ICD10CM:H90.3
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Disease

Diseases --> Human genes

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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