All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05207 OCA1 albinism, oculocutaneous, type I (OCA-1) - - 212 212 TYR - -
00473 OCA1A albinism, oculocutaneous, type IA (OCA-1A) 203100 AR 299 299 TYR - -
00474 OCA1B albinism, oculocutaneous, type IB (OCA-1B) 606952 AR 43 43 TYR - -
00479 OCA3 albinism, oculocutaneous, type III (OCA-3) 203290 AR 9 7 TYRP1 - -
00032 PLOSL1 polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL) 221770 AR - - TREM2, TYROBP - -
00480 SHEP11 pigmentation, eyes, blue/non-blue, type 11 (SHEP-11, Melanesian blond hair, skin/hair/eye pigmentation) 612271 - - - TYRP1 - -
00476 SHEP3 pigmentation, eye, blue/green - skin, light/dark/freckling, type 3 (SHEP-3, skin/hair/eye pigmentation) 601800 AD - - TYR - -
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