Disease #02514 (CAMT (thrombocytopenia, amegakaryocytic, congenital (CAMT)))

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Zeynep Tümer

Official abbreviation	CAMT
Name	thrombocytopenia, amegakaryocytic, congenital (CAMT)
OMIM ID	-
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	MPL, THPO
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2023-09-01 13:08:02 +02:00 (CEST)

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