Disease #00132 (MDS (myelodysplastic syndrome (MDS)), OMIM:614286)
| Official abbreviation |
MDS |
| Name |
myelodysplastic syndrome (MDS) |
| OMIM ID |
614286 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Somatic mosaicism |
| Individuals reported having this disease |
10 |
| Phenotype entries for this disease |
13 |
| Associated with 5 genes |
ASXL1, GATA2, PTPN11, SF3B1, TET2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-05-17 15:26:22 +02:00 (CEST) |
| Date last edited |
2024-05-24 16:19:35 +02:00 (CEST) |
Individuals
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