Lujan Fryns syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The Lujan-Fryns syndrome or X-linked mental retardation (XLMR) with marfanoid habitus syndrome is a syndromic X-linked form of intellectual disability, associated with tall, marfanoid stature, distinct facial dysmorphism and behavioral problems. (Orphanet Rare Disease Ontology, Orphanet_776)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537724
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Genes

1 genes/proteins associated with the disease Lujan Fryns syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MED12 mediator complex subunit 12 2.88009