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
|