NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Noonan-like syndrome with loose anagen hair (NS/LAH) is a Noonan related syndrome, characterized by facial anomalies suggestive of Noonan syndrome (see this term); distinctive hair anomaly described as loose anagen hair syndrome (see this term); frequent congenital heart defects; distinctive skin features with darkly pigmented skin, keratosis pilaris, eczema or occasional neonatal ichtyosis (see this term); short stature often associated with a GH deficiency and psychomotor delays. (Orphanet Rare Disease Ontology, Orphanet_2701)
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:607721
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Genes

1 genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SHOC2 soc-2 suppressor of clear homolog (C. elegans) 2.88009