Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the skin (HP:0000951)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Abnormality of subcutaneous fat tissue (HP:0001001)help
Parent Node:
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Multiple lipomas (HP:0001012)help
Parent Node:
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Neoplasm of the skin (HP:0008069)help
..Starting node
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Subcutaneous lipoma (HP:0001031)help
Term ID: 1031
Name: Subcutaneous lipoma
Synonym:
Definition: The presence of subcutaneous lipoma.
Comments:
Reference: HP:0001031
Genes and Diseases:
 
       Child Nodes:
........expandPainful subcutaneous lipomas (HP:0007596) help

 Sister Nodes: 
..expandAcanthoma (HP:0025432) help
..expandActinic keratosis (HP:0025127) help
..expandAdenoma sebaceum (HP:0009720) help
..expandBasal cell carcinoma (HP:0002671) help
..expandCutaneous angiolipomas (HP:0006773) help
..expandCutaneous leiomyoma (HP:0007620) help
..expandCutaneous leiomyosarcoma (HP:0006755) help
..expandCutaneous mastocytosis (HP:0200151) help
..expandCutaneous melanoma (HP:0012056) help
..expandCutaneous myxoma (HP:0030428) help
..expandEccrine syringofibroadenoma (HP:0031018) help
..expandFibrofolliculoma (HP:0030436) help
..expandFrontal cutaneous lipoma (HP:0007541) help
..expandKaposi's sarcoma (HP:0100726) help
..expandKeratoacanthoma (HP:0031525) help
..expandLymphocytoma cutis (HP:0031549) help
..expandMerkel cell skin cancer (HP:0030447) help
..expandMultiple cutaneous leiomyomas (HP:0007437) help
..expandMultiple cutaneous malignancies (HP:0007606) help
..expandMyxoid subcutaneous tumors (HP:0006769) help
..expandNeurofibromas (HP:0001067) help
..expandPapilloma (HP:0012740) help
..expandPeripheral Schwannoma (HP:0009593) help
..expandSeborrheic keratosis (HP:0031287) help
..expandSkin appendage neoplasm (HP:0012842) help
..expandSquamous cell carcinoma (HP:0002860) help
..expandSteatocystoma multiplex (HP:0012035) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001031HP:0001031Subcutaneous lipoma0AKT1 CL E G H207615109Cowden syndrome 6615109C3554519OMIM112391164730
HP:0001031HP:0001031Subcutaneous lipoma0CDKN1A CL E G H1026652AmebiasisORPHA181784116899
HP:0001031HP:0001031Subcutaneous lipoma0CDKN1B CL E G H1027276152ORPHA1251785600778
HP:0001031HP:0001031Subcutaneous lipoma0CDKN1B CL E G H1027652AmebiasisORPHA1251785600778
HP:0001031HP:0001031Subcutaneous lipoma0CDKN2B CL E G H1030652AmebiasisORPHA1141788600431
HP:0001031HP:0001031Subcutaneous lipoma0CDKN2C CL E G H1031652AmebiasisORPHA121789603369
HP:0001031HP:0001031Subcutaneous lipoma0FGFR1 CL E G H2260613001Encephalocraniocutaneous lipomatosis613001C0406612OMIM12653688136350
HP:0001031HP:0001031Subcutaneous lipoma0MEN1 CL E G H4221652AmebiasisORPHA17487010613733
HP:0001031HP:0001031Subcutaneous lipoma0MEN1 CL E G H4221131100Multiple endocrine neoplasia, type 1131100C0025267OMIM17487010613733
HP:0001031HP:0001031Subcutaneous lipoma0PIK3CA CL E G H5290615108Cowden syndrome 5615108C3554518OMIM1578975171834
HP:0001031HP:0001031Subcutaneous lipoma0PTEN CL E G H57282969ORPHA16589588601728
HP:0001031HP:0001031Subcutaneous lipoma0PTEN CL E G H5728158350Cowden syndrome 1158350CN072330OMIM16589588601728
HP:0001031HP:0001031Subcutaneous lipoma1AKT1 CL E G H207615109Cowden syndrome 6615109C3554519OMIM112391164730
HP:0001031HP:0001031Subcutaneous lipoma1CDKN1A CL E G H1026652AmebiasisORPHA181784116899
HP:0001031HP:0001031Subcutaneous lipoma1CDKN1B CL E G H1027276152ORPHA1251785600778
HP:0001031HP:0001031Subcutaneous lipoma1CDKN1B CL E G H1027652AmebiasisORPHA1251785600778
HP:0001031HP:0001031Subcutaneous lipoma1CDKN2B CL E G H1030652AmebiasisORPHA1141788600431
HP:0001031HP:0001031Subcutaneous lipoma1CDKN2C CL E G H1031652AmebiasisORPHA121789603369
HP:0001031HP:0001031Subcutaneous lipoma1FGFR1 CL E G H2260613001Encephalocraniocutaneous lipomatosis613001C0406612OMIM12653688136350
HP:0001031HP:0001031Subcutaneous lipoma1MEN1 CL E G H4221652AmebiasisORPHA17487010613733
HP:0001031HP:0001031Subcutaneous lipoma1MEN1 CL E G H4221131100Multiple endocrine neoplasia, type 1131100C0025267OMIM17487010613733
HP:0001031HP:0001031Subcutaneous lipoma1PIK3CA CL E G H5290615108Cowden syndrome 5615108C3554518OMIM1578975171834
HP:0001031HP:0001031Subcutaneous lipoma1PTEN CL E G H57282969ORPHA16589588601728
HP:0001031HP:0001031Subcutaneous lipoma1PTEN CL E G H5728158350Cowden syndrome 1158350CN072330OMIM16589588601728
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (9) :AKT1 CDKN1A CDKN1B CDKN2B CDKN2C FGFR1 MEN1 PIK3CA PTEN

Diseases (8) :615109 652 276152 613001 131100 615108 2969 158350
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.