Nonspherocytic hemolytic anemia

Symptom Information:

Symptom ID: HPO:0001930
Synonyms:
Nonspherocytic hemolytic anemia [OMIM:Nonspherocytic hemolytic anemia]
Nonspherocytic hemolytic anemia (Dacie's type II) [OMIM:Nonspherocytic hemolytic anemia (Dacie's type II)]
Quality:
Cross references:
OMIM: "Nonspherocytic hemolytic anemia" [OMIM:Nonspherocytic hemolytic anemia]
OMIM: "Nonspherocytic hemolytic anemia (Dacie's type II)" [OMIM:Nonspherocytic hemolytic anemia (Dacie's type II)]
Is a (Direct Parents):
HPO         Hemolytic anemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Anemia(HPO:0001903)
                Anemia due to reduced life span of red cells(HPO:0011895)
                   Hemolytic anemia(HPO:0001878)
                      Nonspherocytic hemolytic anemia(HPO:0001930)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF REDCELL MEMBRANE (OMIM:206300)
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRINMETABOLISM (OMIM:206400)
Anemia due to adenosine triphosphatase deficiency (Orphanet:1044)
Glycogen storage disease due to aldolase A deficiency (Orphanet:57)
Heinz body anemia (Orphanet:178330)
Hemolytic anemia due to diphosphoglycerate mutase deficiency (Orphanet:714)
Hemolytic anemia due to glucophosphate isomerase deficiency (Orphanet:712)
Hereditary pyropoikilocytosis (Orphanet:98867)
Non-spherocytic hemolytic anemia due to hexokinase deficiency (Orphanet:90031)
Triose phosphate-isomerase deficiency (Orphanet:868)