Abnormal hemoglobin
Symptom Information:
Symptom ID: | HPO:0011902 | ||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||
Cross references: |
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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) Abnormal hemoglobin(HPO:0011902) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormal hemoglobin(HPO:0011902) |
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Database Frequency: | 18 / 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) |
Beta-thalassemia | (Orphanet:848) |
Beta-thalassemia - X-linked thrombocytopenia | (Orphanet:231393) |
Beta-thalassemia associated with another hemoglobin anomaly | (Orphanet:231230) |
Beta-thalassemia intermedia | (Orphanet:231222) |
Beta-thalassemia major | (Orphanet:231214) |
Congenital amegakaryocytic thrombocytopenia | (Orphanet:3319) |
Delta-beta-thalassemia | (Orphanet:231237) |
Dominant beta-thalassemia | (Orphanet:231226) |
HEMOGLOBIN--ZETA LOCUS | (OMIM:142310) |
Hb Bart's hydrops fetalis | (Orphanet:163596) |
Hemoglobin C - beta-thalassemia | (Orphanet:231242) |
Hemoglobin E - beta-thalassemia | (Orphanet:231249) |
Hereditary persistence of fetal hemoglobin - beta-thalassemia | (Orphanet:46532) |
Pearson syndrome | (Orphanet:699) |
Primary familial polycythemia | (Orphanet:90042) |