Child syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description CHILD syndrome (Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects, CS) is an X-linked dominant genodermatosis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies. (Orphanet Rare Disease Ontology, Orphanet_139)
External Link http://www.omim.org/entry/308050
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Child syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
NSDHL NAD(P) dependent steroid dehydrogenase-like