Disease #00806 (MLC2B (leukoencephalopathy, megalencephalic with subcortical cysts 2B, remitting, with/without mental retardation, type 2B (MLC2B)), OMIM:613926)

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Official abbreviation	MLC2B
Name	leukoencephalopathy, megalencephalic with subcortical cysts 2B, remitting, with/without mental retardation, type 2B (MLC2B)
OMIM ID	613926
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HEPACAM
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-05-18 10:08:23 +02:00 (CEST)

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