Subcutaneous nodule

Symptom Information:

Symptom ID: HPO:0001482
Synonyms:
Multiple, subcutaneous nodules [HPO:0001482]
Subcutaneous nodules [HPO:0001482]
Subcutaneous nodule (finding) [Orphanet:23730]
Subcutaneous nodule [Orphanet:23730]
Subcutaneous nodules [OMIM:Subcutaneous nodules]
Subcutaneous nodules/lipomas/tumefaction/swelling [Orphanet:23730]
Skin mass [MedDRA:10067868]
Fibrous nodule [MedDRA:10067868]
Nodule skin [MedDRA:10067868]
Nodule subcutaneous [MedDRA:10067868]
Phyma [MedDRA:10067868]
Skin nodule [MedDRA:10067868]
Subcutaneous nodule [MedDRA:10067868]
Fibrous nodules [OMIM:Fibrous nodules]
Subcutaneous nodules (fingers) [OMIM:Subcutaneous nodules (fingers)]
Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial) [OMIM:Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial)]
Quality:
Cross references:
Orphanet:23730 "Subcutaneous nodules/lipomas/tumefaction/swelling" [Orphanet:23730]
OMIM: "Subcutaneous nodules" [OMIM:Subcutaneous nodules]
OMIM: "Fibrous nodules" [OMIM:Fibrous nodules]
OMIM: "Subcutaneous nodules (fingers)" [OMIM:Subcutaneous nodules (fingers)]
OMIM: "Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial)" [OMIM:Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial)]
UMLS:C0151811 "Subcutaneous nodule" [Orphanet:23730]
Is a (Direct Parents):
HPO         Skin nodule
Orphanet Neoplasm of the skin
MedDRA Skin and subcutaneous conditions NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Localized skin lesion(HPO:0011355)
                Skin nodule(HPO:0200036)
                   Subcutaneous nodule(HPO:0001482)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue disorders NEC(MedDRA:10040790)
       Skin and subcutaneous conditions NEC(MedDRA:10042356)
          Subcutaneous nodule(HPO:0001482)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS (OMIM:108050)
Buschke-Ollendorff syndrome (Orphanet:1306)
Carney complex (Orphanet:1359)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Insulin-resistance syndrome type A (Orphanet:2297)
Juvenile hyaline fibromatosis (Orphanet:2028)
KNUCKLE PADS (OMIM:149100)
MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY (OMIM:259600)
Oculocerebrorenal syndrome (Orphanet:534)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
RHEUMATOID NODULOSIS (OMIM:180350)
Rosaï-Dorfman disease (Orphanet:158014)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Torg-Winchester syndrome (Orphanet:3460)
Tuberous sclerosis (Orphanet:805)