Nonspherocytic hemolytic anemia
Symptom Information:
Symptom ID: | HPO:0001930 | ||
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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: |
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Database Frequency: | 10 / 7739 | ||
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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) |