Human Phenotype Ontology 
Grandparent Node:
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Neoplasm (HP:0002664)help
Parent Node:
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Abnormal heart morphology (HP:0001627)help
Parent Node:
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Neoplasm by anatomical site (HP:0011793)help
..Starting node
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Neoplasm of the heart (HP:0100544)help
Term ID: 100544
Name: Neoplasm of the heart
Synonym: Cardiac neoplasia; Cardiac neoplasm; Heart tumor
Definition: A tumor (abnormal growth of tissue) of the heart.
Comments:
Reference: HP:0100544
Genes and Diseases:
 
       Child Nodes:
........expandCardiac rhabdomyoma (HP:0009729) help
........expandCardiac fibroma (HP:0010617) help
........expandCardiac myxoma (HP:0011672) help
........expandCardiac hemangioma (HP:0011673) help
........expandCardiac teratoma (HP:0011674) help
........expandCardiac sarcoma (HP:0031350) help
........expandCalcified amorphous tumor of the heart (HP:0031351) help

 Sister Nodes: 
..expandHematological neoplasm (HP:0004377) help
..expandMalignant mesothelioma (HP:0100001) help
..expandNeoplasm of fatty tissue (HP:0200013) 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 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:0100544HP:0100544Neoplasm of the heart0ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA020145102545
HP:0100544HP:0100544Neoplasm of the heart0LMOD1 CL E G H258022241Factor XI deficiency, congenitalORPHA016647602715
HP:0100544HP:0100544Neoplasm of the heart0MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA0697569160745
HP:0100544HP:0100544Neoplasm of the heart0MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA0437590600922
HP:0100544HP:0100544Neoplasm of the heart1ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA020145102545
HP:0100544HP:0100544Neoplasm of the heart1LMOD1 CL E G H258022241Factor XI deficiency, congenitalORPHA016647602715
HP:0100544HP:0100544Neoplasm of the heart1MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA0697569160745
HP:0100544HP:0100544Neoplasm of the heart1MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA0437590600922


Genes (11) :ACTG2 LMOD1 MYH11 MYH8 MYLK PRKAR1A PTCH1 PTCH2 SUFU TSC1 TSC2

Diseases (9) :2241 608837 1359 615 77301 109400 805 191100 613254
 

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