Human Phenotype Ontology 
Grandparent Node:
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Neoplasm by histology (HP:0011792)help
Parent Node:
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Neoplasm of the skeletal system (HP:0010622)help
Parent Node:
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Sarcoma (HP:0100242)help
..Starting node
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Chondrosarcoma (HP:0006765)help
Term ID: 6765
Name: Chondrosarcoma
Synonym:
Definition: A slowly growing malignant neoplasm derived from cartilage cells.
Comments:
Reference: HP:0006765
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEwing sarcoma (HP:0012254) help
..expandOsteosarcoma (HP:0002669) help
..expandRenal sarcoma (HP:0008663) help
..expandSoft tissue sarcoma (HP:0030448) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H2131215300Chondrosarcoma215300C0008479OMIM15243512608177
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H2131215300Chondrosarcoma215300C0008479OMIM16483512608177
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H2131133700Multiple congenital exostosis133700C0015306OMIM15243512608177
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H2131133700Multiple congenital exostosis133700C0015306OMIM16483512608177
HP:0006765HP:0006765Chondrosarcoma0EXT2 CL E G H2132133701Multiple exostoses type 2133701C1851413OMIM14663513608210
HP:0006765HP:0006765Chondrosarcoma0EXT2 CL E G H2132133701Multiple exostoses type 2133701C1851413OMIM13793513608210
HP:0006765HP:0006765Chondrosarcoma0NR4A3 CL E G H8013612237Epithelial-myoepithelial carcinoma612237C1275278OMIM1377982600542
HP:0006765HP:0006765Chondrosarcoma0NR4A3 CL E G H8013612237Epithelial-myoepithelial carcinoma612237C1275278OMIM1367982600542
HP:0006765HP:0006765Chondrosarcoma0TAF15 CL E G H8148612237Epithelial-myoepithelial carcinoma612237C1275278OMIM18511547601574
HP:0006765HP:0006765Chondrosarcoma0TAF15 CL E G H8148612237Epithelial-myoepithelial carcinoma612237C1275278OMIM18611547601574
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H2131321ORPHA05243512608177
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H2131321ORPHA06483512608177
HP:0006765HP:0006765Chondrosarcoma0EXT2 CL E G H2132321ORPHA04663513608210
HP:0006765HP:0006765Chondrosarcoma0EXT2 CL E G H2132321ORPHA03793513608210
HP:0006765HP:0006765Chondrosarcoma0IDH1 CL E G H3417163634ORPHA0685382147700
HP:0006765HP:0006765Chondrosarcoma0IDH1 CL E G H3417296ORPHA0695382147700
HP:0006765HP:0006765Chondrosarcoma0IDH1 CL E G H3417296ORPHA0685382147700
HP:0006765HP:0006765Chondrosarcoma0IDH1 CL E G H3417163634ORPHA0695382147700
HP:0006765HP:0006765Chondrosarcoma0IDH2 CL E G H3418296ORPHA01405383147650
HP:0006765HP:0006765Chondrosarcoma0IDH2 CL E G H3418163634ORPHA01625383147650
HP:0006765HP:0006765Chondrosarcoma0IDH2 CL E G H3418163634ORPHA01405383147650
HP:0006765HP:0006765Chondrosarcoma0IDH2 CL E G H3418296ORPHA01625383147650
HP:0006765HP:0006765Chondrosarcoma0PTH1R CL E G H5745296ORPHA01669608168468
HP:0006765HP:0006765Chondrosarcoma0PTH1R CL E G H5745296ORPHA01359608168468


Genes (7) :EXT1 EXT2 IDH1 IDH2 NR4A3 PTH1R TAF15

Diseases (7) :321 215300 133700 133701 296 163634 612237
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.