Human Phenotype Ontology 
Grandparent Node:
Abnormal heart morphology (HP:0001627)help
Grandparent Node:
Neoplasm by anatomical site (HP:0011793)help
Parent Node:
Fibroma (HP:0010614)help
Parent Node:
Neoplasm of the heart (HP:0100544)help
..Starting node
Cardiac fibroma (HP:0010617)help
Term ID: 10617
Name: Cardiac fibroma
Definition: A fibroma of the heart.
Reference: HP:0010617
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandCalcified amorphous tumor of the heart (HP:0031351) help
..expandCardiac hemangioma (HP:0011673) help
..expandCardiac myxoma (HP:0011672) help
..expandCardiac rhabdomyoma (HP:0009729) help
..expandCardiac sarcoma (HP:0031350) help
..expandCardiac teratoma (HP:0011674) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0010617HP:0010617Cardiac fibroma0PTCH1 CL E G H572777301ORPHA15299585601309
HP:0010617HP:0010617Cardiac fibroma0PTCH1 CL E G H5727109400Gorlin syndrome109400C0004779OMIM15299585601309
HP:0010617HP:0010617Cardiac fibroma0PTCH2 CL E G H8643109400Gorlin syndrome109400C0004779OMIM1119586603673
HP:0010617HP:0010617Cardiac fibroma0SUFU CL E G H51684109400Gorlin syndrome109400C0004779OMIM14716466607035
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (3) :PTCH1 PTCH2 SUFU

Diseases (2) :77301 109400

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