| 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 |
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 |
