Human Phenotype Ontology 
Grandparent Node:
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Neoplasm (HP:0002664)help
Parent Node:
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Abnormal adipose tissue morphology (HP:0009124)help
Parent Node:
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Neoplasm by anatomical site (HP:0011793)help
..Starting node
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Neoplasm of fatty tissue (HP:0200013)help
Term ID: 200013
Name: Neoplasm of fatty tissue
Synonym: Tumor of fatty tissue
Definition: A tumor (abnormal growth of tissue) of adipose tissue.
Comments:
Reference: HP:0200013
Genes and Diseases:
 
       Child Nodes:
........expandLipomatous tumor (HP:0012031) help
................... HP:0001012 Multiple lipomas
................... HP:0012032 Lipoma
................... HP:0012034 Liposarcoma

 Sister Nodes: 
..expandHematological neoplasm (HP:0004377) help
..expandMalignant mesothelioma (HP:0100001) help
..expandNeoplasm of head and neck (HP:0012288) help
..expandNeoplasm of striated muscle (HP:0009728) help
..expandNeoplasm of the breast (HP:0100013) help
..expandNeoplasm of the ear (HP:0012780) help
..expandNeoplasm of the endocrine system (HP:0100568) help
..expandNeoplasm of the eye (HP:0100012) help
..expandNeoplasm of the gastrointestinal tract (HP:0007378) help
..expandNeoplasm of the genitourinary tract (HP:0007379) help
..expandNeoplasm of the heart (HP:0100544) help
..expandNeoplasm of the lip (HP:0100604) help
..expandNeoplasm of the nail (HP:0100826) help
..expandNeoplasm of the nervous system (HP:0004375) help
..expandNeoplasm of the oral cavity (HP:0100649) help
..expandNeoplasm of the pancreas (HP:0002894) help
..expandNeoplasm of the respiratory system (HP:0100606) help
..expandNeoplasm of the skeletal system (HP:0010622) help
..expandNeoplasm of the skin (HP:0008069) help
..expandNeoplasm of the thymus (HP:0100521) help
..expandRetroperitoneal chemodectomas (HP:0006729) help
..expandSoft tissue neoplasm (HP:0031459) help
..expandVascular neoplasm (HP:0100742) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0200013HP:0200013Neoplasm of fatty tissue0 CL E G H
HP:0200013HP:0200013Neoplasm of fatty tissue1 CL E G H
HP:0200013HP:0200013Neoplasm of fatty tissue2 CL E G H
HP:0200013HP:0200013Neoplasm of fatty tissue3 CL E G H
HP:0200013HP:0200013Neoplasm of fatty tissue4 CL E G H
HP:0200013HP:0200013Neoplasm of fatty tissue5 CL E G H


Genes (49) :ABCC6 AKT1 ALX1 ALX3 AP2S1 APC CDC73 CDKN1A CDKN1B CDKN2B CDKN2C COX1 COX2 COX3 ENPP1 FGFR1 FLCN GNA11 KLLN KRAS LEMD3 MEN1 MFN2 MSTO1 ND1 ND4 ND5 ND6 PIK3CA PTEN RNR1 RPL10 SDHB SDHC SDHD SEC23B SPRED1 TRNF TRNH TRNK TRNL1 TRNP TRNQ TRNS1 TRNS2 TRNW VANGL1 VANGL2 ZSWIM6

Diseases (41) :758 201 744 176920 600740 79665 247806 175100 99880 143 550 2396 613001 122 135150 145981 1879 2398 502423 617675 551 276280 612918 109 611431 1349 182940 603671 615109 136760 652 276152 131100 615108 2969 158350 435938 600145 1827 306542 391474
 

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