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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 multiple lipomatosis 
fibrodysplasia ossificans progressiva 
FLOTCH syndrome 
FLOTCH syndrome is a rare, genetic, cutaneous disorder characterized by leuchonychia and multiple, recurrent pilar cysts, associated or not with ciliar dystrophy and/or koilonychia. Renal calculi have also been reported.
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:2045 ;   http://identifiers.org/medgen/419074 ;   http://identifiers.org/mesh/C537065 ;   http://linkedlifedata.com/resource/umls/id/C2931411 ;   leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome
Related Synonyms: familial occurrence of total leukonychia, trichilemmal cysts and ciliary dystrophy with dominant autosomal heredity
Alternate IDs: MONDO:0016083
Xrefs: GARD:2346 ;   MEDGEN:419074 ;   MESH:C537065 ;   ORDO:2045 ;   UMLS:C2931411
see_also: https://rarediseases.info.nih.gov/diseases/2346/flotch-syndrome" xsd:anyURI {source="GARD:0002346
Definition Sources: Orphanet:2045

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