Disease #00713 (MCPH-4 (microcephaly, type 4, primary, autosomal recessive (MCPH-4)), OMIM:604321)

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Official abbreviation	MCPH-4
Name	microcephaly, type 4, primary, autosomal recessive (MCPH-4)
OMIM ID	604321
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	CASC5, CEP152
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A