Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the endocrine system (HP:0000818)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Abnormality of the parathyroid morphology (HP:0011766)help
Parent Node:
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Neoplasm of the endocrine system (HP:0100568)help
..Starting node
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Neoplasm of the parathyroid gland (HP:0100733)help
Term ID: 100733
Name: Neoplasm of the parathyroid gland
Synonym: Parathyroid neoplasia
Definition: A tumor (abnormal growth of tissue) of the parathyroid gland.
Comments:
Reference: HP:0100733
Genes and Diseases:
 
       Child Nodes:
........expandParathyroid adenoma (HP:0002897) help
........expandParathyroid carcinoma (HP:0006780) help

 Sister Nodes: 
..expandAPUdoma (HP:0040192) help
..expandNeoplasm of the adrenal gland (HP:0100631) help
..expandNeoplasm of the pituitary gland (HP:0040277) help
..expandNeoplasm of the thyroid gland (HP:0100031) help
..expandNeuroendocrine neoplasm (HP:0100634) 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:0100733HP:0100733Neoplasm of the parathyroid gland0 CL E G H
HP:0100733HP:0100733Neoplasm of the parathyroid gland1 CL E G H


Genes (13) :CDC73 CDKN1A CDKN1B CDKN2B CDKN2C FLCN GCM2 IDH1 IDH2 MEN1 NF1 PRKAR1A RET

Diseases (15) :99879 143 99880 145001 608266 652 276152 610755 122 617343 163634 131100 162200 1359 171400
 

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