Search Ontology:
Human Disease

Usher syndrome type 1

Term ID
DOID:0110826
Synonyms
  • US1
  • USH1
Definition
An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa. (3)
References
  • GARD:5435
  • ICD10CM:H35.5
  • MIM:276900
  • NCI:C126327
  • ORDO:231169
  • UMLS_CUI:C1568247
Ontology
Human Disease   ( DOID:0110826 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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