Disease #01117 (mental retardation, X-linked syndromic, Fried type, OMIM:300630)

Official abbreviation -
Name mental retardation, X-linked syndromic, Fried type
OMIM ID 300630
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene AP1S2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2015-12-08 23:50:05 +01:00 (CET)

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