Human Phenotype Ontology 
Grandparent Node:
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Neoplasm (HP:0002664)help
Parent Node:
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Abnormality of the musculature (HP:0003011)help
Parent Node:
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Neoplasm by anatomical site (HP:0011793)help
..Starting node
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Neoplasm of striated muscle (HP:0009728)help
Term ID: 9728
Name: Neoplasm of striated muscle
Synonym: Tumors of striated muscle
Definition: A benign or malignant neoplasm (tumour) originating in striated muscle, either skeletal muscle or cardiac muscle.
Comments:
Reference: HP:0009728
Genes and Diseases:
 
       Child Nodes:
........expandRhabdomyosarcoma (HP:0002859) help
................... HP:0006743 Embryonal rhabdomyosarcoma
................... HP:0006779 Alveolar rhabdomyosarcoma
................... HP:0500092 Orbital rhabdomyosarcoma
........expandRhabdomyoma (HP:0009730) help
................... HP:0009729 Cardiac rhabdomyoma

 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 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 heart (HP:0100544) 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:0009728HP:0009728Neoplasm of striated muscle0 CL E G H
HP:0009728HP:0009728Neoplasm of striated muscle1 CL E G H
HP:0009728HP:0009728Neoplasm of striated muscle2 CL E G H


Genes (25) :BUB1 BUB1B BUB3 CEP57 DICER1 FOXO1 HRAS KEAP1 MC1R MLH1 MSH2 MSH6 NBN NF1 NRAS PAX3 PAX7 PMS2 PTCH1 PTCH2 SLC22A18 SUFU TRIP13 TSC1 TSC2

Diseases (18) :1052 257300 601200 218040 626 276300 647 251260 162200 77301 276399 180295 268220 109400 268210 805 191100 613254
 

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