Lipomatosis, familial multiple

Preferred Label : Lipomatosis, familial multiple;

Symbol : FML;

CISMeF acronym : FML; LIPO;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Lipomatosis, multiple; LIPO; Lipoma;

Description : Familial multiple lipomatosis is a rare autosomal dominant disorder characterized by numerous encapsulated lipomas on the trunk and extremities (Keskin et al., 2002).;

Inheritance : Autosomal dominant;

Prefixed ID : %151900;

Details

Origin ID

151900;

UMLS CUI

C1275273;

Automatic exact mappings (from CISMeF team)
- FML [MeSH concept]
- Familial Multiple Lipomatosis [MeSH concept]
- HMGA2 wt Allele [NCIt concept]
- High-Mobility Group Protein HMGI-C [NCIt concept]
- LIPOMA [WHO-ART Preferred Term]
- Lipoma [PASCAL descriptor]
- Lipoma [ICD-11 Subcategory]
- Lipoma [HPO term]
- Lipoma [ICD-9 code]
- Lipoma [MedDRA Preferred Term]
- Lipoma [NCIt concept]
- Lipoma (disorder) [SNOMED CT concept]
- Lipoma NOS [MedDRA LLT]
- Lipoma, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- Multiple lipomas [HPO term]
- Smooth muscle cell [FMA entity]
- high mobility group AT-hook 2 [ORDO Gene]
- lipoma [DO Concept]
- lipoma [ICPC-2 Rubric]
- lipoma [MeSH Descriptor]
- lipoma [MeSH concept]
- lipoma [Radlex concept]
- lipoma, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Familial Multiple Lipomatosis [MeSH Descriptor]
- Familial multiple lipomatosis [MedDRA Preferred Term]
- Familial multiple lipomatosis [ORDO Disease]
- Familial multiple lipomatosis (disorder) [SNOMED CT concept]
- lipomatosis, multiple [MeSH concept]
DO Cross reference
- lipoma [DO Concept]
- multiple symmetric lipomatosis [DO Concept]
False automatic mappings
- fluorometholone [MeSH Descriptor]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Multiple lipomas [HPO term]
ORDO concept(s)
- Familial multiple lipomatosis [ORDO Disease]
See also inter- (CISMeF)
- lipoma [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Multiple Lipomatosis [MeSH Descriptor]
- Familial multiple lipomata (disorder) [SNOMED CT concept]
- Familial multiple lipomatosis [ORDO Disease]
- Familial multiple lipomatosis [MedDRA Preferred Term]
- Familial multiple lipomatosis (disorder) [SNOMED CT concept]
- lipomatosis, multiple [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients