Multiple lipomas

Symptom Information:

Symptom ID: HPO:0001012
Synonyms:
Lipomas [HPO:0001012]
Lipoma [Orphanet:23700]
Lipoma (disorder) [Orphanet:23700]
Lipomas [OMIM:Lipomas]
Xanthomas/lipomas [Orphanet:23700]
Lipoma [MedDRA:10024612]
Lipoma NOS [MedDRA:10024612]
Lipoma of intra-abdominal organs [MedDRA:10024612]
Lipoma of intrathoracic organs [MedDRA:10024612]
Lipoma of other skin and subcutaneous tissue [MedDRA:10024612]
Lipoma of other specified sites [MedDRA:10024612]
Lipoma of skin and subcutaneous tissue of face [MedDRA:10024612]
Lipoma of spermatic cord [MedDRA:10024612]
Lipoma, unspecified site [MedDRA:10024612]
Multiple lipomata [OMIM:Multiple lipomata]
Quality:
Cross references:
HPO:0012032 "Lipoma" [Orphanet:23700]
Orphanet:23700 "Xanthomas/lipomas" [Orphanet:23700]
OMIM: "Lipomas" [OMIM:Lipomas]
OMIM: "Multiple lipomata" [OMIM:Multiple lipomata]
UMLS:C0023798 "Lipoma" [Orphanet:23700]
Is a (Direct Parents):
Orphanet Xanthomatosis
Orphanet Neoplasm of the skin
MedDRA Soft tissue neoplasms benign NEC
HPO         Lipomatous tumor
HPO         Lipomas of upper eyelids
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of fatty tissue(HPO:0200013)
                Lipomatous tumor(HPO:0012031)
                   Multiple lipomas(HPO:0001012)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Soft tissue neoplasms benign(MedDRA:10041294)
       Soft tissue neoplasms benign NEC(MedDRA:10041295)
          Multiple lipomas(HPO:0001012)
Database Frequency: 43 / 7739
Resource:

All diseases associated with this symptom:

APC-related attenuated familial adenomatous polyposis (Orphanet:247806)
Aicardi syndrome (Orphanet:50)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Attenuated familial adenomatous polyposis (Orphanet:220460)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Birt-Hogg-Dube syndrome (Orphanet:122)
Cerebrotendinous xanthomatosis (Orphanet:909)
Cholestasis - lymphedema (Orphanet:1414)
Cholesteryl ester storage disease (Orphanet:75234)
Cleft lip/palate - deafness - sacral lipoma (Orphanet:2003)
Cobb syndrome (Orphanet:53721)
Cowden syndrome (Orphanet:201)
DISORGANIZATION, MOUSE, HOMOLOG OF (OMIM:223200)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Erdheim-Chester disease (Orphanet:35687)
Extensor tendons of finger anomalies (Orphanet:3294)
Familial adenomatous polyposis (Orphanet:733)
Familial hypocalciuric hypercalcemia type 2 (Orphanet:101049)
Familial hypocalciuric hypercalcemia type 3 (Orphanet:101050)
Familial multiple lipomatosis (Orphanet:199276)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
Familial symmetric lipomatosis (Orphanet:2398)
Gardner syndrome (Orphanet:79665)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Hypoalphalipoproteinemia (Orphanet:31153)
Legius syndrome (Orphanet:137605)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
Melorheostosis with osteopoikilosis (Orphanet:1879)
Multiple endocrine neoplasia type 1 (Orphanet:652)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Neural tube closure defect (Orphanet:268357)
Neurofibromatosis type 1 (Orphanet:636)
Primary lipodystrophy (Orphanet:90970)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Pseudoxanthoma elasticum (Orphanet:758)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Turcot syndrome with polyposis (Orphanet:99818)
Wolman disease (Orphanet:75233)