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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|