All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00002 RP (XL) Retinitis Pigmentosa (X-linked) - XL 2 0 CHM, GPR143, MED12, OFD1, RP2, RPGR, RS1 - -
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