Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness

Term ID
DOID:0050565
Synonyms
Definition
A nonsyndromic deafness characterized by an autosomal recessive inheritance mode. http://ghr.nlm.nih.gov/condition/nonsyndromic-deafness
References
  • ICD10CM:H90.3
  • MIM:607197
  • MIM:PS220290
  • ORDO:90636
Ontology
Human Disease   ( DOID:0050565 )
Relationships
is a type of
has subtype
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Genes Involved
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