Human Phenotype Ontology 
Grandparent Node:
Neoplasm by histology (HP:0011792)help
Parent Node:
Neoplasm of the skeletal system (HP:0010622)help
Parent Node:
Sarcoma (HP:0100242)help
..Starting node
Chondrosarcoma (HP:0006765)help
Term ID: 6765
Name: Chondrosarcoma
Definition: A slowly growing malignant neoplasm derived from cartilage cells.
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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H21313512OMIM:215300Chondrosarcoma.96
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H21313512OMIM:133700Exostoses, multiple, type I.96
HP:0006765HP:0006765Chondrosarcoma0EXT1 CL E G H21313512ORPHA:321Multiple osteochondromasHP:0040284 - Very rare96
HP:0006765HP:0006765Chondrosarcoma0EXT2 CL E G H21323513OMIM:133701Exostoses, multiple, type II.102
HP:0006765HP:0006765Chondrosarcoma0EXT2 CL E G H21323513ORPHA:321Multiple osteochondromasHP:0040284 - Very rare102
HP:0006765HP:0006765Chondrosarcoma0IDH1 CL E G H34175382ORPHA:163634Maffucci syndromeHP:0040283 - Occasional15
HP:0006765HP:0006765Chondrosarcoma0IDH1 CL E G H34175382ORPHA:296Ollier diseaseHP:0040283 - Occasional15
HP:0006765HP:0006765Chondrosarcoma0IDH2 CL E G H34185383ORPHA:163634Maffucci syndromeHP:0040283 - Occasional29
HP:0006765HP:0006765Chondrosarcoma0IDH2 CL E G H34185383ORPHA:296Ollier diseaseHP:0040283 - Occasional29
HP:0006765HP:0006765Chondrosarcoma0NR4A3 CL E G H80137982OMIM:612237Chondrosarcoma, extraskeletal myxoid.
HP:0006765HP:0006765Chondrosarcoma0PTH1R CL E G H57459608ORPHA:296Ollier diseaseHP:0040283 - Occasional58
HP:0006765HP:0006765Chondrosarcoma0TAF15 CL E G H814811547OMIM:612237Chondrosarcoma, extraskeletal myxoid.

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

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

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.