Phenotypes for disease #00014 (G6PD (G6PD deficiency), OMIM:305900)

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

Phenotype details     

Inheritance     

Owner     

Individual ID     
0000000226 acute hemolysis, favism, hyperbilimbinemia, neonatal jaundice - Nur Aisyah Athirah 00000637
0000000227 acute hemolysis, favism, hyperbilimbinemia, neonatal jaundice - Nur Aisyah Athirah 00000638
0000000228 acute hemolysis, favism, hyperbilimbinemia, neonatal jaundice - Nur Aisyah Athirah 00000639
0000000315 dark-coloured urine and pallor since birth - Noorzalifah Binti Mazuki 00000839
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