Term Name: Legius syndrome
Synonyms: LGSS, neurofibromatosis type 1-like syndrome, NF1-like syndrome
Definition: A RASopathy characterized by multiple cafe-au-lait macules and possible skin fold freckling without neurofibromas, optic gliomas, or Lisch nodules that has_material_basis_in heterozygous mutation in the SPRED1 gene on chromosome 15q14.
Ontology: Human Disease [DOID:0070484]   ( DOID:0070484 )

Relationships
is a type of: autosomal dominant disease RASopathy