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.

This is just here as a test because I lose it

Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=791
hasDbXref
  • OMIM:268025
  • OMIM:609913
  • OMIM:618195
  • OMIM:612095
  • OMIM:613582
  • OMIM:617023
  • OMIM:613581
  • OMIM:617781
  • OMIM:617304
  • OMIM:613341
  • OMIM:613861
  • OMIM:608380
  • OMIM:613464
  • OMIM:615922
  • OMIM:613862
  • OMIM:613983
  • OMIM:610599
  • OMIM:610359
  • OMIM:600132
  • MeSH:D012174
  • OMIM:600138
  • OMIM:613194
  • OMIM:616188
  • OMIM:613750
  • OMIM:617433
  • OMIM:616469
  • OMIM:612943
  • OMIM:613756
  • OMIM:613758
  • OMIM:608133
  • OMIM:268000
  • MedDRA:10038914
  • OMIM:615780
  • OMIM:612712
  • OMIM:613801
  • OMIM:312612
  • OMIM:613767
  • OMIM:606068
  • OMIM:613769
  • OMIM:613809
  • OMIM:602772
  • OMIM:614180
  • OMIM:614181
  • OMIM:612165
  • OMIM:615434
  • OMIM:618826
  • OMIM:613810
  • OMIM:614500
  • OMIM:312600
  • OMIM:604393
  • ICD-10:H35.5
  • UMLS:C0035334
  • OMIM:617460
  • OMIM:600105
  • OMIM:601718
  • OMIM:615565
  • OMIM:618955
  • OMIM:612572
  • OMIM:613660
  • OMIM:619007
  • OMIM:268060
  • OMIM:180210
  • OMIM:615725
  • OMIM:613428
  • OMIM:613827
  • OMIM:602594
  • OMIM:600059
  • OMIM:600852
  • OMIM:607921
  • OMIM:610282
  • OMIM:616544
  • OMIM:611131
  • OMIM:300605
  • OMIM:613794
  • OMIM:180100
  • OMIM:180104
  • OMIM:180105
  • OMIM:300424
  • OMIM:616394
  • OMIM:601414
  • OMIM:618697
  • OMIM:618173
  • OMIM:614494
  • OMIM:617123
  • OMIM:300029
  • OMIM:618613
  • OMIM:609923
  • OMIM:300155
  • OMIM:618345
  • OMIM:616562
  • OMIM:618220
  • OMIM:400004
  • OMIM:613575
  • OMIM:615233
  • OMIM:613731
  • OMIM:604232
  • OMIM:613617
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409948
  • http://www.orpha.net/ORDO/Orphanet_409947
  • http://www.orpha.net/ORDO/Orphanet_409946
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
  • http://www.orpha.net/ORDO/Orphanet_409933
  • http://www.orpha.net/ORDO/Orphanet_409932
  • http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence average value
  • 22.5
  • 20.5
  • 21.0
  • 30.0
  • 16.7
  • 26.7
  • 26.4
  • 11.09
  • 25.4
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409975
notation
  • ORPHA:791
part of
  • http://www.orpha.net/ORDO/Orphanet_519306
  • http://www.orpha.net/ORDO/Orphanet_156171
  • http://www.orpha.net/ORDO/Orphanet_611314
  • http://www.orpha.net/ORDO/Orphanet_156168
present in
  • http://www.orpha.net/ORDO/Orphanet_409991
  • http://www.orpha.net/ORDO/Orphanet_410037
  • http://www.orpha.net/ORDO/Orphanet_410224
  • http://www.orpha.net/ORDO/Orphanet_410157
  • http://www.orpha.net/ORDO/Orphanet_410225
  • http://www.orpha.net/ORDO/Orphanet_410109
  • http://www.orpha.net/ORDO/Orphanet_410051
  • http://www.orpha.net/ORDO/Orphanet_410193
  • http://www.orpha.net/ORDO/Orphanet_409984

Term relations

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