Disease #00065 (Rett syndrome, congenital variant, OMIM:613454)

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Official abbreviation	-
Name	Rett syndrome, congenital variant
OMIM ID	613454
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FOXG1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-10-31 14:44:58 +01:00 (CET)
Date last edited	N/A