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Disease Ontology Browser
linear nevus sebaceous syndrome (DOID:0111530)
Alliance: disease page
Synonyms: Jadassohn nevus phakomatosis; JNP; nevus sebaceus of Jadassohn; nevus sebaceus syndrome; organoid nevus phakomatosis; organoid nevus syndrome; Schimmelpenning Feuerstein Mims syndrome; Schimmelpenning syndrome; SFM syndrome; Solomon syndrome
Alt IDs: OMIM:163200, ORDO:2612, UMLS_CUI:C3854181
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory