Disease #07163 (MCPH27 (microcephaly, type 27, primary, autosomal dominant), OMIM:619180)

Global Variome shared LOVD

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Official abbreviation	MCPH27
Name	microcephaly, type 27, primary, autosomal dominant
OMIM ID	619180
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LMNB2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-04-17 19:24:57 +02:00 (CEST)
Date last edited	N/A

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