Subcutaneous tissue disorder

Summary

Subcutaneous tissue disorder (MONDO:0019296) is a disease (an umbrella term covering 19 Mondo subtypes). 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: 19 Mondo subtypes

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	subcutaneous tissue disorder
Mondo ID	MONDO:0019296
Orphanet	79382
UMLS	C1290008
MedGen	712397
Anatomy (UBERON)	UBERON:0011818
Is cancer (heuristic)	no

Also known as: disease of superficial fascia · disease or disorder of superficial fascia · disorder of superficial fascia · superficial fascia disease · superficial fascia disease or disorder

Disease family

An umbrella term covering 19 Mondo subtypes.

Classification path: disease › human disease › disease by body system or component › integumentary system disorder › subcutaneous tissue disorder

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, panniculitis, 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, Bartholin gland neoplasm, pseudoxanthoma elasticum (inherited or acquired), skin appendage disorder, keratinization disease, paraneoplastic cutaneous syndrome

Subtypes (19): nodular fasciitis, hemangioma of subcutaneous tissue, adiposis dolorosa, isolated anhidrosis with normal sweat glands, fibrodysplasia ossificans progressiva, multiple symmetric lipomatosis, familial multiple lipomatosis, familial angiolipomatosis, cerebrotendinous xanthomatosis, dissecting cellulitis of the scalp, Pierpont syndrome, CLOVES syndrome, encephalocraniocutaneous lipomatosis, Lipedema, FLOTCH syndrome, mycetoma, nodular non-suppurative panniculitis, Roch-Leri mesosomatous lipomatosis, cytophagic histiocytic panniculitis

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: 0.