Hypochromic anemia
Symptom Information:
Symptom ID: | HPO:0001931 | ||
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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) Hypochromic anemia(HPO:0001931) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Congenital atransferrinemia | (Orphanet:1195) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS | (OMIM:257790) |