Hypochromic microcytic anemia
Symptom Information:
Symptom ID: | HPO:0004840 | |||||
Synonyms: |
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Is a (Direct Parents): |
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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) Microcytic anemia(HPO:0001935) Hypochromic microcytic anemia(HPO:0004840) Hypochromic anemia(HPO:0001931) Hypochromic microcytic anemia(HPO:0004840) MedDRA: |
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Database Frequency: | 15 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Alpha-thalassemia | (Orphanet:846) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
Beta-thalassemia major | (Orphanet:231214) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
HEMOGLOBIN--ALPHA LOCUS 1 | (OMIM:141800) |
IRIDA syndrome | (Orphanet:209981) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS,AND DEVELOPMENTAL DELAY | (OMIM:616084) |
X-linked sideroblastic anemia | (Orphanet:75563) |
X-linked sideroblastic anemia - ataxia | (Orphanet:2802) |