Panniculitis
diseaseOn this page
Also known as inflammation of subcutaneous adipose tissueSubcutaneous adipose tissuesubcutaneous adipose tissue inflammationSubcutaneous tissuesubcutis
Summary
Panniculitis (MONDO:0006591) is a disease (an umbrella term covering 6 Mondo subtypes) and 7 clinical trials. A subtype of integumentary system disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Umbrella term: 6 Mondo subtypes
- Clinical trials: 7
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | panniculitis |
| Mondo ID | MONDO:0006591 |
| EFO | EFO:1000746 |
| MeSH | D015434 |
| DOID | DOID:1526 |
| ICD-11 | 1056888958 |
| NCIT | C33645 |
| SNOMED CT | 22125009 |
| UMLS | C0030326 |
| MedGen | 45301 |
| Is cancer (heuristic) | no |
Also known as: inflammation of subcutaneous adipose tissue · Subcutaneous adipose tissue · subcutaneous adipose tissue inflammation · Subcutaneous tissue · subcutis
Disease family
An umbrella term covering 6 Mondo subtypes.
Classification path: disease › human disease › disease by body system or component › integumentary system disorder › panniculitis
Related subtypes (35): Neu-Laxova syndrome, cutaneous mycosis, integumentary system benign neoplasm, integumentary system cancer, nipple neoplasm, nail disorder, disorder of pilosebaceous unit, Bartholin duct cyst, benign mammary dysplasia, skin disorder, breast fibrosis, breast mucosa-associated lymphoid tissue lymphoma, alopecia-epilepsy-pyorrhea-intellectual disability syndrome, autosomal dominant deafness - onychodystrophy syndrome, keratoderma hereditarium mutilans, Rombo syndrome, Sjogren-Larsson syndrome, mucosulfatidosis, ichthyosis prematurity syndrome, ANE syndrome, frontonasal dysplasia with alopecia and genital anomaly, peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome, mandibulofacial dysostosis with alopecia, cutis laxa, X-linked ichthyosis syndrome, demodicidosis, Proteus-like syndrome, familial atypical multiple mole melanoma syndrome, familial tumoral calcinosis, subcutaneous tissue disorder, Bartholin gland neoplasm, pseudoxanthoma elasticum (inherited or acquired), skin appendage disorder, keratinization disease, paraneoplastic cutaneous syndrome
Subtypes (6): nodular non-suppurative panniculitis, panniculitis and localized lipodystrophy, lupus erythematosus panniculitis, cytophagic histiocytic panniculitis, lipodermatosclerosis, erythema nodosum
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 7.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 7 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06838988 | Not specified | RECRUITING | Ultrasonographic Patterns and Pathological Correlation in the Diagnosis of Subcutaneous Nodules |
| NCT07027033 | Not specified | RECRUITING | Nutritional Oleic Acid Modulation of adIpose Cholesterol Metabolism in Patients Living With Obesity |
| NCT07345949 | Not specified | RECRUITING | Panniculitis in Dermatomyositis |
| NCT01464658 | Not specified | TERMINATED | Prospective Study of Functional and Quality of Life Outcomes in Panniculectomy Patients |
| NCT01853397 | Not specified | COMPLETED | Evaluation of the Treatment of Adipose Tissue With Liposonix System (Model 2) Using a New Treatment Method |
| NCT01952275 | Not specified | UNKNOWN | Observational Study of the Genetic Architecture of Neutrophil-Mediated Inflammatory Skin Diseases |
| NCT03785990 | Not specified | UNKNOWN | Fatty Acid Composition of Subcutaneous Adipose Tissue in Infants: A Prospective and Observational Study |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.