Multiple lipomas
Symptom Information:
Symptom ID: | HPO:0001012 | |||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |