Symptom Information: Sort according to HPO 

1
 (HPO:0000961) Cyanosis 60 / 7739
2
 (HPO:0001871) Abnormality of blood and blood-forming tissues 37 / 7739
3
 (OMIM) Sulfhemoglobinemia 1 / 7739
4
 (OMIM) Congenital cyanosis 1 / 7739
5
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739