|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the Child syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|NSDHL||NAD(P) dependent steroid dehydrogenase-like|