| Dataset | OMIM Gene-Disease 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 |
1 genes associated with the child syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| NSDHL | NAD(P) dependent steroid dehydrogenase-like |
