Microcytic anemia
Symptom Information:
| Symptom ID: | HPO:0001935 | ||||||||
| 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) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Anaemias nonhaemolytic and marrow depression(MedDRA:10002086) Anaemias NEC(MedDRA:10002067) Microcytic anemia(HPO:0001935) |
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| Database Frequency: | 32 / 7739 | ||||||||
| Resource: |
All diseases associated with this symptom:
| Alpha-thalassemia | (Orphanet:846) |
| Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
| Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
| Beta-thalassemia | (Orphanet:848) |
| Beta-thalassemia associated with another hemoglobin anomaly | (Orphanet:231230) |
| Beta-thalassemia intermedia | (Orphanet:231222) |
| Beta-thalassemia major | (Orphanet:231214) |
| Blue rubber bleb nevus | (Orphanet:1059) |
| CANDLE syndrome | (Orphanet:325004) |
| Central nervous system calcification - deafness - tubular acidosis - anemia | (Orphanet:3240) |
| Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
| DK1-CDG | (Orphanet:91131) |
| Delta-beta-thalassemia | (Orphanet:231237) |
| Dermatitis herpetiformis | (Orphanet:1656) |
| Dominant beta-thalassemia | (Orphanet:231226) |
| Erythropoietic protoporphyria | (Orphanet:79278) |
| HEMOGLOBIN--BETA LOCUS | (OMIM:141900) |
| Hemochromatosis type 4 | (Orphanet:139491) |
| Hemoglobin C - beta-thalassemia | (Orphanet:231242) |
| Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
| JMP syndrome | (Orphanet:324999) |
| Klippel-Trénaunay syndrome | (Orphanet:90308) |
| Lesch-Nyhan syndrome | (Orphanet:510) |
| Majeed syndrome | (Orphanet:77297) |
| Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
| Nakajo-Nishimura syndrome | (Orphanet:2615) |
| Niemann-Pick disease type A | (Orphanet:77292) |
| Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
| Proteasome disability syndrome | (Orphanet:324977) |
| SRD5A3-CDG | (Orphanet:324737) |
| Wiskott-Aldrich syndrome | (Orphanet:906) |
| Wolfram syndrome 2 | (OMIM:604928) |