Normocytic anemia

Symptom Information:

Symptom ID: HPO:0001897
Synonyms:
Normocytic anemia (disorder) [Orphanet:48240]
Normocytic anemia [Orphanet:48240]
Normocytic anemia [OMIM:Normocytic anemia]
Normochromic normocytic anaemia [MedDRA:10029783]
Anaemia normochromic [MedDRA:10029783]
Anaemia normocytic [MedDRA:10029783]
Anemia normochromic [MedDRA:10029783]
Anemia normocytic [MedDRA:10029783]
Normochromic anaemia [MedDRA:10029783]
Normocytic anaemia [MedDRA:10029783]
Normocytic anemia [MedDRA:10029783]
Normochromic anemia [MedDRA:10029783]
Normochromic normocytic anemia [MedDRA:10029783]
Quality:
Cross references:
Orphanet:48240 "Normocytic anemia" [Orphanet:48240]
OMIM: "Normocytic anemia" [OMIM:Normocytic anemia]
UMLS:C0085577 "Normocytic anemia" [Orphanet:48240]
Is a (Direct Parents):
HPO         Anemia of inadequate production
MedDRA Anaemias NEC
Orphanet 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 of inadequate production(HPO:0010972)
                   Normocytic anemia(HPO:0001897)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Anaemias nonhaemolytic and marrow depression(MedDRA:10002086)
       Anaemias NEC(MedDRA:10002067)
          Normocytic anemia(HPO:0001897)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

DIAMOND-BLACKFAN ANEMIA 13 (OMIM:615909)
Familial LCAT deficiency (Orphanet:79293)
Glycogen storage disease due to aldolase A deficiency (Orphanet:57)
Hemolytic anemia due to diphosphoglycerate mutase deficiency (Orphanet:714)
Non-spherocytic hemolytic anemia due to hexokinase deficiency (Orphanet:90031)
Triose phosphate-isomerase deficiency (Orphanet:868)
Waldenström macroglobulinemia (Orphanet:33226)