|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Legius syndrome, also known as NF1-like syndrome, is a rare, genetic, skin pigmentation disorder characterized by multiple café-au-lait macules with or without axillary or inguinal freckling. (Orphanet Rare Disease Ontology, Orphanet_137605)|
|Downloads & Tools|
1 genes associated with the Legius syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|SPRED1||sprouty-related, EVH1 domain containing 1|