Disease #04400 (MCPH12 (microcephaly?, type 12, primary, autosomal recessive (MCPH-12)), OMIM:616080)

Global Variome shared LOVD

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Official abbreviation	MCPH12
Name	microcephaly?, type 12, primary, autosomal recessive (MCPH-12)
OMIM ID	616080
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CDK6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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