Select a disease to view all phenotype entries

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00001 alpha-thal alpha thalassemia 604131 - 1011 1010 HBA1, HBA2 - -
00002 beta-thal beta thalassemia 613985 - 1306 1027 HBB - -
00006 Hypochromic anemia Microcytic hypochromic anemia - - 3 3 KLF1 - -
00018 PKD Paroxysmal kinesigenic dyskinesia - AD 1 1 PRRT2, TMEM151A - -
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