Disease #00393 (MCPH-1 (microcephaly, type 1, primary, autosomal recessive (MCPH-1)), OMIM:251200)

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Official abbreviation	MCPH-1
Name	microcephaly, type 1, primary, autosomal recessive (MCPH-1)
OMIM ID	251200
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MCPH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-05-30 09:28:05 +02:00 (CEST)
Date last edited	N/A