Abnormality of bone marrow cell morphology
Symptom Information:
Symptom ID: | HPO:0005561 | ||||
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 bone marrow cell morphology(HPO:0005561) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Aggressive systemic mastocytosis | (Orphanet:98850) |
Classical mycosis fungoides | (Orphanet:2584) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Essential thrombocythemia | (Orphanet:3318) |
Gaucher disease type 1 | (Orphanet:77259) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Pachydermoperiostosis | (Orphanet:2796) |
Reticular dysgenesis | (Orphanet:33355) |
Schnitzler syndrome | (Orphanet:37748) |
Sialidosis type 2 | (Orphanet:87876) |
WHIM syndrome | (Orphanet:51636) |