Human Phenotype Ontology 
Grandparent Node:
Sarcoma (HP:0100242)help
Parent Node:
Soft tissue sarcoma (HP:0030448)help
..Starting node
Angiosarcoma (HP:0200058)help
Term ID: 200058
Name: Angiosarcoma
Reference: HP:0200058
Genes and Diseases:
       Child Nodes:
........expandMetastatic angiosarcoma (HP:0200059) help

 Sister Nodes: 
..expandAlveolar soft part sarcoma (HP:0012218) help
..expandFibroma (HP:0010614) help
..expandFibrosarcoma (HP:0100244) help
..expandLeiomyosarcoma (HP:0100243) help
..expandNeurofibrosarcoma (HP:0100697) help
..expandRhabdomyosarcoma (HP:0002859) help
..expandSynovial sarcoma (HP:0012570) 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:0200058HP:0200058Angiosarcoma0EPHB4 CL E G H20503395ORPHA:90186Meige diseaseHP:0040283 - Occasional3
HP:0200058HP:0200058Angiosarcoma0FLT4 CL E G H23243767ORPHA:79452Milroy diseaseHP:0040283 - Occasional90
HP:0200058HP:0200058Angiosarcoma0GJC2 CL E G H5716517494ORPHA:79452Milroy diseaseHP:0040283 - Occasional37
HP:0200058HP:0200059Metastatic angiosarcoma1 CL E G H

Genes (3) :EPHB4 FLT4 GJC2

Diseases (2) :ORPHA:90186 ORPHA:79452

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