Subcutaneous lipoma

Symptom Information:

Symptom ID: HPO:0001031
Synonyms:
Subcutaneous lipomas [OMIM:Subcutaneous lipomas]
Quality:
Cross references:
OMIM: "Subcutaneous lipomas" [OMIM:Subcutaneous lipomas]
Is a (Direct Parents):
HPO         Abnormality of subcutaneous fat tissue
HPO         Multiple lipomas
HPO         Neoplasm of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Neoplasm of the skin(HPO:0008069)
                Subcutaneous lipoma(HPO:0001031)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of subcutaneous fat tissue(HPO:0001001)
                   Subcutaneous lipoma(HPO:0001031)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skin(HPO:0008069)
                Subcutaneous lipoma(HPO:0001031)
             Neoplasm of fatty tissue(HPO:0200013)
                Lipomatous tumor(HPO:0012031)
                   Multiple lipomas(HPO:0001012)
                      Subcutaneous lipoma(HPO:0001031)
       Abnormality of connective tissue(HPO:0003549)
          Abnormality of adipose tissue(HPO:0009124)
             Abnormality of subcutaneous fat tissue(HPO:0001001)
                Subcutaneous lipoma(HPO:0001031)
MedDRA:
Database Frequency: 112 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
Acrokeratoelastoidosis of Costa (Orphanet:38)
Adiposis dolorosa (Orphanet:36397)
Aggressive systemic mastocytosis (Orphanet:98850)
Albright hereditary osteodystrophy (Orphanet:665)
Alport syndrome (Orphanet:63)
Amelogenesis imperfecta and gingival hyperplasia syndrome (Orphanet:171836)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Behçet disease (Orphanet:117)
Benign cephalic histiocytosis (Orphanet:157997)
Blue rubber bleb nevus (Orphanet:1059)
COWDEN SYNDROME 5 (OMIM:615108)
COWDEN SYNDROME 6 (OMIM:615109)
Chylous ascites (Orphanet:1160)
Cowden syndrome (Orphanet:201)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cutaneous lupus erythematosus (Orphanet:535)
Cutaneous mastocytoma (Orphanet:79455)
Cutaneous mastocytosis (Orphanet:66646)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Dermatofibrosarcoma protuberans (Orphanet:31112)
Desmoid tumor (Orphanet:873)
Dissecting cellulitis of the scalp (Orphanet:345)
Dracunculiasis (Orphanet:231)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Enchondromatosis (Orphanet:296)
Eosinophilic fasciitis (Orphanet:3165)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erythema elevatum diutinum (Orphanet:90000)
Fabry disease (Orphanet:324)
Familial Dupuytren contracture (Orphanet:79142)
Familial cutaneous collagenoma (Orphanet:53296)
Familial cylindromatosis (Orphanet:211)
Familial keratoacanthoma (Orphanet:493)
Familial multiple trichoepithelioma (Orphanet:867)
Farber lipogranulomatosis (Orphanet:333)
Felty syndrome (Orphanet:47612)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Focal dermal hypoplasia (Orphanet:2092)
Fountain syndrome (Orphanet:3219)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Gorlin syndrome (Orphanet:377)
Hairy cell leukemia variant (Orphanet:300878)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Hennekam-Beemer syndrome (Orphanet:2135)
Hyaluronidase deficiency (Orphanet:67041)
Infantile myofibromatosis (Orphanet:2591)
Isolated osteopoikilosis (Orphanet:166119)
Juvenile Paget disease (Orphanet:2801)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile hyaline fibromatosis (Orphanet:2028)
Juvenile xanthogranuloma (Orphanet:158000)
Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome (Orphanet:2698)
Large congenital melanocytic nevus (Orphanet:626)
Lassa fever (Orphanet:99824)
Ledderhose disease (Orphanet:199251)
Leri pleonosteosis (Orphanet:2900)
Lhermitte-Duclos disease (Orphanet:65285)
Lipedema (Orphanet:77243)
Lipoid proteinosis (Orphanet:530)
Liposarcoma (Orphanet:69078)
Lyme disease (Orphanet:91546)
Maculopapular cutaneous mastocytosis (Orphanet:79457)
Maffucci syndrome (Orphanet:163634)
Malakoplakia (Orphanet:556)
Median nodule of the upper lip (Orphanet:2699)
Melorheostosis with osteopoikilosis (Orphanet:1879)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Microscopic polyangiitis (Orphanet:727)
Multiple endocrine neoplasia type 1 (Orphanet:652)
Myxoid/round cell liposarcoma (Orphanet:99967)
Nakajo-Nishimura syndrome (Orphanet:2615)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Neurofibromatosis type 1 (Orphanet:636)
Neurofibromatosis type 2 (Orphanet:637)
Nodular non-suppurative panniculitis (Orphanet:33577)
Noonan syndrome with multiple lentigines (Orphanet:500)
PTEN hamartoma tumor syndrome (Orphanet:306498)
Pai syndrome (Orphanet:1993)
Papular xanthoma (Orphanet:158008)
Pleomorphic liposarcoma (Orphanet:99969)
Porokeratosis (Orphanet:79358)
Primary cutaneous anaplastic large cell lymphoma (Orphanet:300865)
Primary cutaneous lymphoma (Orphanet:542)
Progressive nodular histiocytosis (Orphanet:158022)
Progressive osseous heteroplasia (Orphanet:2762)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Pseudoxanthoma elasticum (Orphanet:758)
Pyoderma gangrenosum (Orphanet:48104)
Pyomyositis (Orphanet:764)
Relapsing polychondritis (Orphanet:728)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Rhabdoid tumor (Orphanet:69077)
Rheumatic fever (Orphanet:3099)
Roch-Leri mesosomatous lipomatosis (Orphanet:529)
Scleroderma (Orphanet:801)
Sea-blue histiocytosis (Orphanet:158029)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
Stiff skin syndrome (Orphanet:2833)
Sweet syndrome (Orphanet:3243)
Syringocystadenoma papilliferum (Orphanet:840)
Takayasu arteritis (Orphanet:3287)
Torg-Winchester syndrome (Orphanet:3460)
Townes-Brocks syndrome (Orphanet:857)
Tuberous sclerosis (Orphanet:805)
Tumoral calcinosis (Orphanet:53715)
Well-differentiated liposarcoma (Orphanet:99971)
Wells syndrome (Orphanet:901)