Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 10
HPO ID | Term | Frequency |
---|---|---|
HP:0002863 | Myelodysplasia | Very frequent (99-80%) |
HP:0001871 | Abnormality of blood and blood-forming tissues | Frequent (79-30%) |
HP:0012148 | Multiple lineage myelodysplasia | Frequent (79-30%) |
HP:0012378 | Fatigue | Frequent (79-30%) |
HP:0045040 | Abnormal lactate dehydrogenase activity | Frequent (79-30%) |
HP:0001974 | Leukocytosis | Occasional (29-5%) |
HP:0002960 | Autoimmunity | Occasional (29-5%) |
HP:0005528 | Bone marrow hypocellularity | Occasional (29-5%) |
HP:0030166 | Night sweats | Occasional (29-5%) |
HP:0004808 | Acute myeloid leukemia | Very rare (4-1%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|