Disease #00857 (MCPH-10 (microcephaly, type 10, primary, autosomal recessive (MCPH-10)), OMIM:615095)

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Official abbreviation	MCPH-10
Name	microcephaly, type 10, primary, autosomal recessive (MCPH-10)
OMIM ID	615095
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ZNF335
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A