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Usher syndrome

^ http://www.orpha.net/ORDO/Orphanet_886


Usher syndrome (US) is characterized by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.

Synonyms: Retinitis pigmentosa-deafness syndrome, USH

Term info

database cross reference
  • ICD-10:H35.5 (NTBT (narrower term maps to a broader term))
  • OMIM:500004 (BTNT (broader term maps to a narrower term))
  • OMIM:606943 (BTNT (broader term maps to a narrower term))
  • OMIM:614990 (BTNT (broader term maps to a narrower term))
  • OMIM:276900 (BTNT (broader term maps to a narrower term))
  • OMIM:605472 (BTNT (broader term maps to a narrower term))
  • OMIM:276901 (BTNT (broader term maps to a narrower term))
  • MeSH:D052245 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:276902 (BTNT (broader term maps to a narrower term))
  • OMIM:614504 (BTNT (broader term maps to a narrower term))
  • OMIM:612632 (BTNT (broader term maps to a narrower term))
  • UMLS:C0271097 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:614869 (BTNT (broader term maps to a narrower term))
  • MedDRA:10063396 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:611383 (BTNT (broader term maps to a narrower term))
  • OMIM:602083 (BTNT (broader term maps to a narrower term))
  • OMIM:601067 (BTNT (broader term maps to a narrower term))
  • OMIM:276904 (BTNT (broader term maps to a narrower term))
  • OMIM:602097 (BTNT (broader term maps to a narrower term))
  • ICD-10:H35.5 (Attributed)
hasDbXref

OMIM:276904, OMIM:601067, OMIM:606943, ICD-10:H35.5, OMIM:276900, OMIM:276901, OMIM:276902, OMIM:500004, OMIM:614990, OMIM:611383, MedDRA:10063396, MeSH:D052245, OMIM:612632, OMIM:614869, OMIM:605472, OMIM:602083, UMLS:C0271097, OMIM:614504, OMIM:602097

notation

ORPHA:886

Term relations

Subclass of: