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DOID:0111530 - linear nevus sebaceous syndrome
Disease Ontology Definition:A syndrome characterized by sebaceous nevi typically on the face and associated with variable ipsilateral abnormalities of the central nervous system, ocular anomalies, and skeletal defects that has_material_basis_in somatic mosaic mutations in the NRAS, HRAS, or KRAS genes on chromosomes 1p13.2, 11p15.5, or 12p12.1, respectively.
Synonyms: JNP, Jadassohn nevus phakomatosis, SFM syndrome, Schimmelpenning Feuerstein Mims syndrome, Schimmelpenning syndrome, Solomon syndrome, nevus sebaceus of Jadassohn, nevus sebaceus syndrome, organoid nevus phakomatosis, organoid nevus syndrome,
Echinobase Genes
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Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)