Human Phenotype Ontology 
Grandparent Node:
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Neoplasm (HP:0002664)help
Parent Node:
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Abnormality of the thymus (HP:0000777)help
Parent Node:
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Neoplasm by anatomical site (HP:0011793)help
..Starting node
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Neoplasm of the thymus (HP:0100521)help
Term ID: 100521
Name: Neoplasm of the thymus
Synonym:
Definition: A tumor (abnormal growth of tissue) of the thymus.
Comments:
Reference: HP:0100521
Genes and Diseases:
 
       Child Nodes:
........expandThymoma (HP:0100522) 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 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
..expandRetroperitoneal chemodectomas (HP:0006729) help
..expandSoft tissue neoplasm (HP:0031459) help
..expandVascular neoplasm (HP:0100742) 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:0100521HP:0100521Neoplasm of the thymus0AKT1 CL E G H207391ORPHA:744Proteus syndromeHP:0040283 - Occasional54
HP:0100521HP:0100521Neoplasm of the thymus0CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 12
HP:0100521HP:0100521Neoplasm of the thymus0CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1102
HP:0100521HP:0100521Neoplasm of the thymus0CDKN1B CL E G H10271785ORPHA:276152Multiple endocrine neoplasia type 4102
HP:0100521HP:0100521Neoplasm of the thymus0CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 11
HP:0100521HP:0100521Neoplasm of the thymus0CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1
HP:0100521HP:0100521Neoplasm of the thymus0MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1462
HP:0100521HP:0100521Neoplasm of the thymus0PTEN CL E G H57289588ORPHA:744Proteus syndromeHP:0040283 - Occasional948
HP:0100521HP:0100522Thymoma1CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare2
HP:0100521HP:0100522Thymoma1CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare102
HP:0100521HP:0100522Thymoma1CDKN1B CL E G H10271785ORPHA:276152Multiple endocrine neoplasia type 4HP:0040284 - Very rare102
HP:0100521HP:0100522Thymoma1CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare1
HP:0100521HP:0100522Thymoma1CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare
HP:0100521HP:0100522Thymoma1MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare462


Genes (7) :AKT1 CDKN1A CDKN1B CDKN2B CDKN2C MEN1 PTEN

Diseases (3) :ORPHA:744 ORPHA:652 ORPHA:276152
 

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