Abnormality of multiple cell lineages in the bone marrow
Symptom Information:
| Symptom ID: | HPO:0012145 | ||
| Synonyms: |
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of bone marrow cell morphology(HPO:0005561) Abnormality of multiple cell lineages in the bone marrow(HPO:0012145) MedDRA: |
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| Database Frequency: | 11 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Chédiak-Higashi syndrome | (Orphanet:167) |
| Follicular lymphoma | (Orphanet:545) |
| Gamma heavy-chain disease | (Orphanet:100026) |
| Hairy cell leukemia variant | (Orphanet:300878) |
| Majeed syndrome | (Orphanet:77297) |
| Mantle cell lymphoma | (Orphanet:52416) |
| Mast cell sarcoma | (Orphanet:66661) |
| Mu heavy-chain disease | (Orphanet:100024) |
| Osteopetrosis | (Orphanet:2781) |
| Pearson syndrome | (Orphanet:699) |
| Waldenström macroglobulinemia | (Orphanet:33226) |