Familial multiple lipomata

disorder

SNOMED 404063007CUI C1275273

Overview

Familial multiple lipomata is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Research Evidence

Peer-reviewed studies linked via MeSH term "Familial Multiple Lipomatosis" from the MEDLINE/PubMed database.

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Subcutaneous Nodules in a Kidney Transplant Recipient: Familial Multiple Lipomatosis.

[object Object], [object Object], [object Object] · Actas Dermosifiliogr · 2017

PMID: 27206607Case Report

Gastroduodenal Lipomatosis in Familial Multiple Lipomatosis.

[object Object], [object Object], [object Object] et al. · Med Princ Pract · 2017

PMID: 27884011Case ReportFull text (PMC)

Cutaneous lipomatosis: diagnosing a rare condition.

[object Object], [object Object], [object Object] · G Ital Dermatol Venereol · 2017

PMID: 29050453Case Report

Multiple symmetric and multiple familial lipomatosis.

[object Object], [object Object], [object Object] et al. · Presse Med · 2021

PMID: 34687914Review

Hyperactivation of the mA demethylase FTO to down-regulate SLC7A11/xCT-mediated redox homeostasis and epigenetic remodeling in facial infiltrating lipomatosis.

[object Object], [object Object], [object Object] et al. · Free Radic Biol Med · 2025

PMID: 40769313Preclinical

Search all PubMed articles for Familial multiple lipomata

Research data from MEDLINE/PubMed

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Subcutaneous lipoma

Very frequent (80-99%)HP:0001031

Cutaneous angiolipomas

Occasional (5-29%)HP:0006773

Obesity

Occasional (5-29%)HP:0001513

Overweight

Occasional (5-29%)HP:0025502

Peripheral neuropathy

Occasional (5-29%)HP:0009830

Painful subcutaneous lipomas

Very rare (1-4%)HP:0007596

Skin calcification

Very rare (1-4%)HP:0007618

Multiple lipomas

HP:0001012

Related Conditions

Multiple lipomata(parent)

Familial neoplastic disease(parent)

Genetic disease(parent)

Quick Facts

SNOMED CT: 404063007
UMLS CUI: C1275273
Fully Specified Name: Familial multiple lipomata (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.