Disease #04402 (MCPH13 (microcephaly?, type 13, primary, autosomal recessive (MCPH-13)), OMIM:616051)

Global Variome shared LOVD

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Official abbreviation	MCPH13
Name	microcephaly?, type 13, primary, autosomal recessive (MCPH-13)
OMIM ID	616051
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CENPE
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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