Symptom Information: Sort according to HPO 

1
(HPO:0000952) Jaundice rare [HPO:skoehler] 105 / 7739
2
(HPO:0000961) Cyanosis 60 / 7739
3
(HPO:0001903) Anemia rare [HPO:skoehler] 289 / 7739
4
(HPO:0001923) Reticulocytosis rare [HPO:skoehler] 28 / 7739
5
(HPO:0002240) Hepatomegaly rare [HPO:skoehler] 467 / 7739
6
(HPO:0012119) Methemoglobinemia 5 / 7739
7
(OMIM) Decreased oxygen-binding capacity of hemoglobin 1 / 7739
8
(OMIM) Decreased hemoglobin oxygen saturation 1 / 7739
9
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
10
(HPO:0003577) Congenital onset 133 / 7739