Disease #07020 (CAMT2 (thrombocytopenia, megakaryocytic, congenital, type 2), OMIM:620481)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CAMT2
Name	thrombocytopenia, megakaryocytic, congenital, type 2
OMIM ID	620481
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	THPO
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-09-01 13:04:36 +02:00 (CEST)
Date last edited	N/A

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