Disease #02514 (CAMT (thrombocytopenia, amegakaryocytic, congenital (CAMT)), OMIM:604498)

MyGenome LOVD - This database is for training purposes only

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

	Curator: Johan T. den Dunnen

Official abbreviation	CAMT
Name	thrombocytopenia, amegakaryocytic, congenital (CAMT)
OMIM ID	604498
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MPL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A