Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Hypoplastic myelodysplasia
Very frequent (80-99%)HP:0002863
Abnormal megakaryocyte morphology
Frequent (30-79%)HP:0012143
Abnormality of red blood cells
Frequent (30-79%)HP:0001877
Bone marrow hypercellularity
Frequent (30-79%)HP:0031020
Erythroid hypoplasia
Frequent (30-79%)HP:0012133
Increased lactate dehydrogenase level
Frequent (30-79%)HP:0025435
Increased platelet count
Frequent (30-79%)HP:0001894
Macrocytic anemia
Frequent (30-79%)HP:0001972
Megakaryocyte nucleus hypolobulation
Frequent (30-79%)HP:0031385
Abnormal neutrophil morphology
Occasional (5-29%)HP:0011992
Abnormality of bone marrow stromal cells
Occasional (5-29%)HP:0012129
Acute myeloid leukaemia
Occasional (5-29%)HP:0004808
Anisocytosis
Occasional (5-29%)HP:0011273
Bleeding tendency
Occasional (5-29%)HP:0001892
Chronic infection
Occasional (5-29%)HP:0031035
Hypoplastic bone marrow
Occasional (5-29%)HP:0005528
Leukopenia
Occasional (5-29%)HP:0001882
Multiple lineage myelodysplasia
Occasional (5-29%)HP:0012148
Ineffective erythropoiesis
HP:0010972
Refractory macrocytic anemia
HP:0004861
Related Conditions
Quick Facts
- SNOMED CT
- 277597005
- UMLS CUI
- C1292779
- Fully Specified Name
- Myelodysplastic syndrome with isolated del(5q) (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.