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.

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Term information

database cross reference
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OMIM:268025

OMIM:609913

OMIM:618195

OMIM:612095

OMIM:617023

OMIM:613582

OMIM:617781

OMIM:613581

OMIM:617304

OMIM:613341

OMIM:613861

OMIM:608380

OMIM:613464

OMIM:613862

OMIM:615922

OMIM:613983

OMIM:610599

OMIM:610359

OMIM:600132

MeSH:D012174

OMIM:600138

OMIM:613194

OMIM:616188

OMIM:617433

OMIM:613750

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:613769

OMIM:606068

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:612572

OMIM:618955

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:611131

OMIM:616544

OMIM:613794

OMIM:300605

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

notation

ORPHA:791

Term relations

Subclass of:

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