Normochromic anemia
Symptom Information:
Symptom ID: | HPO:0001895 | ||
Synonyms: |
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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 of inadequate production(HPO:0010972) Normochromic anemia(HPO:0001895) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
DIAMOND-BLACKFAN ANEMIA 12 | (OMIM:615550) |
Familial LCAT deficiency | (Orphanet:79293) |
Glycogen storage disease due to aldolase A deficiency | (Orphanet:57) |
Hemolytic anemia due to diphosphoglycerate mutase deficiency | (Orphanet:714) |
LCAT deficiency | (Orphanet:650) |
Non-spherocytic hemolytic anemia due to hexokinase deficiency | (Orphanet:90031) |
Triose phosphate-isomerase deficiency | (Orphanet:868) |