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)
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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