Legius syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/611431
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
SPRED1 sprouty-related, EVH1 domain containing 1