Congenital nonspherocytic hemolytic anemia

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Congenital nonspherocytic hemolytic anemia" [OMIM:Congenital nonspherocytic hemolytic anemia]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Glycogen storage disease due to aldolase A deficiency (Orphanet:57)