Disease #00019 (RTT (RETT SYNDROME), OMIM:312750)

Official abbreviation RTT
Name RETT SYNDROME
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 2016-07-08 14:38:01 +00:00 (UTC)
Date last edited N/A

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