integumentary system benign neoplasm lipoma familial multiple lipomatosis SCTID:766888002 MEDGEN:698553 MONDO:0007909 lipomatosis, multiple Orphanet:199276 UMLS:C1275273 ICD9:214.9 DOID:0070518 ICD9:214.8 OMIM:151900 lipoma lipomatosis, familial multiple MESH:D000071070 Familial multiple lipomatosis is a rare, benign, genetic skin disease characterized by numerous, painless, encapsulated lipomas located in the subcutaneous adipose tissue of the trunk and extremities, with relative sparing of the neck and shoulders. Association with gastroduodenal lipomatosis, brain anomalies or lipomatosis, and refractory epilepsy has been reported. GARD:0012925 subcutaneous tissue disorder