Disease #07022 (CAMT1 (thrombocytopenia, megakaryocytic, congenital, type 1), OMIM:604498)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CAMT1
Name	thrombocytopenia, megakaryocytic, congenital, type 1
OMIM ID	604498
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MPL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-09-01 13:08:54 +02:00 (CEST)
Date last edited	N/A

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