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Retinitis pigmentosa

^ http://www.orpha.net/ORDO/Orphanet_791


Retinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades.

Term info

database cross reference
  • OMIM:300424 (BTNT (broader term maps to a narrower term))
  • OMIM:617781 (BTNT (broader term maps to a narrower term))
  • OMIM:613582 (BTNT (broader term maps to a narrower term))
  • OMIM:613617 (BTNT (broader term maps to a narrower term))
  • OMIM:400004 (BTNT (broader term maps to a narrower term))
  • OMIM:612943 (BTNT (broader term maps to a narrower term))
  • OMIM:613827 (BTNT (broader term maps to a narrower term))
  • OMIM:616562 (BTNT (broader term maps to a narrower term))
  • OMIM:615780 (BTNT (broader term maps to a narrower term))
  • OMIM:609923 (BTNT (broader term maps to a narrower term))
  • OMIM:312612 (BTNT (broader term maps to a narrower term))
  • OMIM:600138 (BTNT (broader term maps to a narrower term))
  • OMIM:614180 (BTNT (broader term maps to a narrower term))
  • OMIM:612572 (BTNT (broader term maps to a narrower term))
  • OMIM:617123 (BTNT (broader term maps to a narrower term))
  • OMIM:608380 (BTNT (broader term maps to a narrower term))
  • OMIM:613801 (BTNT (broader term maps to a narrower term))
  • OMIM:606068 (BTNT (broader term maps to a narrower term))
  • OMIM:616188 (ND (not yet decided/unable to decide))
  • OMIM:617023 (BTNT (broader term maps to a narrower term))
  • OMIM:612712 (NTBT (narrower term maps to a broader term))
  • OMIM:613194 (BTNT (broader term maps to a narrower term))
  • OMIM:180100 (BTNT (broader term maps to a narrower term))
  • OMIM:300029 (BTNT (broader term maps to a narrower term))
  • OMIM:610282 (BTNT (broader term maps to a narrower term))
  • OMIM:615233 (BTNT (broader term maps to a narrower term))
  • OMIM:613794 (BTNT (broader term maps to a narrower term))
  • OMIM:613750 (BTNT (broader term maps to a narrower term))
  • OMIM:614181 (BTNT (broader term maps to a narrower term))
  • OMIM:300155 (BTNT (broader term maps to a narrower term))
  • OMIM:609913 (BTNT (broader term maps to a narrower term))
  • OMIM:615565 (BTNT (broader term maps to a narrower term))
  • OMIM:613575 (BTNT (broader term maps to a narrower term))
  • OMIM:613769 (BTNT (broader term maps to a narrower term))
  • OMIM:610359 (BTNT (broader term maps to a narrower term))
  • OMIM:617460 (BTNT (broader term maps to a narrower term))
  • OMIM:268025 (BTNT (broader term maps to a narrower term))
  • OMIM:613862 (BTNT (broader term maps to a narrower term))
  • OMIM:613731 (BTNT (broader term maps to a narrower term))
  • OMIM:300605 (BTNT (broader term maps to a narrower term))
  • MedDRA:10038914 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:615725 (BTNT (broader term maps to a narrower term))
  • OMIM:617304 (BTNT (broader term maps to a narrower term))
  • OMIM:600852 (BTNT (broader term maps to a narrower term))
  • UMLS:C0035334 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:615434 (BTNT (broader term maps to a narrower term))
  • OMIM:180104 (BTNT (broader term maps to a narrower term))
  • OMIM:613767 (BTNT (broader term maps to a narrower term))
  • OMIM:602772 (BTNT (broader term maps to a narrower term))
  • OMIM:616544 (BTNT (broader term maps to a narrower term))
  • OMIM:612165 (BTNT (broader term maps to a narrower term))
  • OMIM:613428 (BTNT (broader term maps to a narrower term))
  • OMIM:600105 (BTNT (broader term maps to a narrower term))
  • ICD-10:H35.5 (NTBT (narrower term maps to a broader term))
  • OMIM:617433 (BTNT (broader term maps to a narrower term))
  • OMIM:616394 (BTNT (broader term maps to a narrower term))
  • OMIM:180105 (BTNT (broader term maps to a narrower term))
  • OMIM:616469 (BTNT (broader term maps to a narrower term))
  • OMIM:608133 (BTNT (broader term maps to a narrower term))
  • OMIM:602594 (BTNT (broader term maps to a narrower term))
  • OMIM:613861 (BTNT (broader term maps to a narrower term))
  • OMIM:613660 (NTBT (narrower term maps to a broader term))
  • OMIM:613810 (BTNT (broader term maps to a narrower term))
  • OMIM:600132 (BTNT (broader term maps to a narrower term))
  • OMIM:604393 (NTBT (narrower term maps to a broader term))
  • OMIM:268000 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:614500 (NTBT (narrower term maps to a broader term))
  • OMIM:613758 (BTNT (broader term maps to a narrower term))
  • OMIM:613464 (BTNT (broader term maps to a narrower term))
  • OMIM:601414 (BTNT (broader term maps to a narrower term))
  • OMIM:613809 (BTNT (broader term maps to a narrower term))
  • OMIM:312600 (BTNT (broader term maps to a narrower term))
  • OMIM:612095 (BTNT (broader term maps to a narrower term))
  • MeSH:D012174 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:613756 (BTNT (broader term maps to a narrower term))
  • OMIM:613341 (NTBT (narrower term maps to a broader term))
  • ICD-10:H35.5 (Inclusion term (The term is included under a ICD10 category and has not its own code))
  • OMIM:614494 (BTNT (broader term maps to a narrower term))
  • OMIM:611131 (BTNT (broader term maps to a narrower term))
  • OMIM:600059 (BTNT (broader term maps to a narrower term))
  • OMIM:607921 (BTNT (broader term maps to a narrower term))
  • OMIM:601718 (BTNT (broader term maps to a narrower term))
  • OMIM:613581 (BTNT (broader term maps to a narrower term))
  • OMIM:604232 (NTBT (narrower term maps to a broader term))
  • OMIM:613983 (BTNT (broader term maps to a narrower term))
  • OMIM:615922 (BTNT (broader term maps to a narrower term))
  • OMIM:268060 (BTNT (broader term maps to a narrower term))
  • OMIM:610599 (BTNT (broader term maps to a narrower term))
  • OMIM:180210 (BTNT (broader term maps to a narrower term))
hasDbXref

OMIM:268025, ICD-10:H35.5, OMIM:609913, UMLS:C0035334, OMIM:617460, OMIM:600105, OMIM:612095, OMIM:601718, OMIM:613582, OMIM:617023, OMIM:617781, OMIM:613581, OMIM:612572, OMIM:617304, OMIM:615565, OMIM:613660, OMIM:613341, OMIM:613861, OMIM:608380, OMIM:613464, OMIM:615922, OMIM:613862, OMIM:613983, OMIM:610599, OMIM:268060, OMIM:610359, OMIM:180210, OMIM:615725, OMIM:613428, OMIM:613827, OMIM:600132, MeSH:D012174, OMIM:602594, OMIM:600059, OMIM:600852, OMIM:607921, OMIM:600138, OMIM:616188, OMIM:613194, OMIM:610282, OMIM:611131, OMIM:616544, OMIM:617433, OMIM:613794, OMIM:613750, OMIM:300605, OMIM:616469, OMIM:612943, OMIM:613756, OMIM:180100, OMIM:613758, OMIM:608133, OMIM:180104, OMIM:180105, OMIM:268000, MedDRA:10038914, OMIM:300424, OMIM:616394, OMIM:601414, OMIM:614494, OMIM:617123, OMIM:300029, OMIM:615780, OMIM:612712, OMIM:613801, OMIM:613767, OMIM:312612, OMIM:613769, OMIM:606068, OMIM:613809, OMIM:602772, OMIM:300155, OMIM:609923, OMIM:614180, OMIM:614181, OMIM:616562, OMIM:400004, OMIM:612165, OMIM:615434, OMIM:615233, OMIM:613575, OMIM:613731, OMIM:613810, OMIM:614500, OMIM:312600, OMIM:604232, OMIM:613617, OMIM:604393

notation

ORPHA:791

Term relations

Subclass of:

Related from:
disease-causing germline mutation(s) in