Disease #05151 (MCPH-9 (microcephaly, type 9, primary, autosomal recessive (MCPH-9)), OMIM:614852)

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Official abbreviation	MCPH-9
Name	microcephaly, type 9, primary, autosomal recessive (MCPH-9)
OMIM ID	614852
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CEP152
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-04-14 15:46:47 +02:00 (CEST)
Date last edited	N/A