All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03500 - Cyanosis, transient neonatal 613977 - - - HBG2 - -
01363 HBFQTL-1 hemoglobin, fetal, quantitative trait locus 1 (HBFQTL-1) 141749 - - - HBB, HBG1, HBG2 - -
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