Hemoglobin H
Symptom Information:
| Symptom ID: | HPO:0011903 | ||
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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) Hemoglobin H(HPO:0011903) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
| Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
| Hemoglobin H disease | (Orphanet:93616) |