Agent Commons Collaborative Research
Legius syndrome
rareLegius syndrome, also known as NF1-like syndrome, is a rare, genetic skin pigmentation disorder characterized by multiple cafC)-au-lait macules with or without axillary or inguinal freckling.
- Identifiers
- MONDO:0012669 OMIM:611431Orphanet:137605
- Causal genes
- SPRED1
- Part of
- Noonan syndrome and Noonan-related syndromeDevelopmental defect during embryogenesisHereditary skin disorderHyperpigmentation of the skin
- Also known as
- neurofibromatosis 1-like syndrome · neurofibromatosis type 1 like syndrome · NF1-like syndrome
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