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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
adiposis dolorosa 
cerebrotendinous xanthomatosis 
CLOVES syndrome 
encephalocraniocutaneous lipomatosis 
familial angiolipomatosis 
Familial angiolipomatosis is a rare, genetic, subcutaneous tissue disorder characterized by the presence of benign, usually multiple, subcutaneous tumors composed of adipose tissue and blood vessels, typically manifesting as yellow, firm, circumscribed, 1-4 cm in diameter tumors located in the arms, legs and trunk, with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures), in several members of a single family. Tumors may be tender or mildly painful when palpated and do not regress spontaneously.
familial multiple lipomatosis 
fibrodysplasia ossificans progressiva 
FLOTCH syndrome 
hemangioma of subcutaneous tissue  
isolated anhidrosis with normal sweat glands 
Lipedema 
multiple symmetric lipomatosis 
nodular fasciitis 
nodular nonsuppurative panniculitis 
Pierpont syndrome 
primary lipodystrophy 
Roch-Leri mesosomatous lipomatosis 

Synonyms
Exact Synonyms: Orphanet:199279 ;   http://identifiers.org/medgen/347235 ;   http://identifiers.org/mesh/C565951 ;   http://linkedlifedata.com/resource/umls/id/C1859784 ;   https://omim.org/entry/206550
Related Synonyms: angiolipoma Microthromboticum
Alternate IDs: MONDO:0008792
Xrefs: GARD:17089 ;   MEDGEN:347235 ;   MESH:C565951 ;   MIM:206550 ;   ORDO:199279 ;   UMLS:C1859784
Definition Sources: Orphanet:199279

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