Disease #00132 (MDS (myelodysplastic syndrome (MDS)), OMIM:614286)

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Official abbreviation	MDS
Name	myelodysplastic syndrome (MDS)
OMIM ID	614286
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 5 genes	ASXL1, EZH2, GATA2, SF3B1, TET2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-05-17 15:26:22 +02:00 (CEST)
Date last edited	N/A