Disease #00066 (RTT (Rett syndrome (RTT)), OMIM:312750)

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Official abbreviation	RTT
Name	Rett syndrome (RTT)
OMIM ID	312750
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MECP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-10-31 15:08:39 +01:00 (CET)
Date last edited	N/A