Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the pituitary gland (HP:0012503)help
Parent Node:
expandAbnormality of the posterior pituitary (HP:0011751)help
..Starting node
..expandNeoplasm of the posterior pituitary (HP:0011752)help
Term ID: 11752
Name: Neoplasm of the posterior pituitary
Synonym: Neoplasm of the neurohypophysis
Definition: The presence of a neoplasm (tumour) in the neurohypophysis, which is also known as the posterior lobe of the hypophysis.
Comments:
Reference: HP:0011752
Genes and Diseases:
 
       Child Nodes:
........expandPituicytoma (HP:0011754) help

 Sister Nodes: 
..expandCentral diabetes insipidus (HP:0000863) help
..expandPosterior pituitary dysgenesis (HP:0011753) 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:0011752HP:0011752Neoplasm of the posterior pituitary0AKT1 CL E G H207391ORPHA:2495MeningiomaHP:0040284 - Very rare54
HP:0011752HP:0011752Neoplasm of the posterior pituitary0BAP1 CL E G H8314950ORPHA:2495MeningiomaHP:0040284 - Very rare184
HP:0011752HP:0011752Neoplasm of the posterior pituitary0NF2 CL E G H47717773ORPHA:2495MeningiomaHP:0040284 - Very rare220
HP:0011752HP:0011752Neoplasm of the posterior pituitary0PDGFB CL E G H51558800ORPHA:2495MeningiomaHP:0040284 - Very rare9
HP:0011752HP:0011752Neoplasm of the posterior pituitary0PIK3CA CL E G H52908975ORPHA:2495MeningiomaHP:0040284 - Very rare162
HP:0011752HP:0011752Neoplasm of the posterior pituitary0SMARCB1 CL E G H659811103ORPHA:2495MeningiomaHP:0040284 - Very rare87
HP:0011752HP:0011752Neoplasm of the posterior pituitary0SMARCE1 CL E G H660511109ORPHA:2495MeningiomaHP:0040284 - Very rare47
HP:0011752HP:0011752Neoplasm of the posterior pituitary0SMO CL E G H660811119ORPHA:2495MeningiomaHP:0040284 - Very rare22
HP:0011752HP:0011752Neoplasm of the posterior pituitary0SUFU CL E G H5168416466ORPHA:2495MeningiomaHP:0040284 - Very rare124
HP:0011752HP:0011752Neoplasm of the posterior pituitary0TERT CL E G H701511730ORPHA:2495MeningiomaHP:0040284 - Very rare238
HP:0011752HP:0011752Neoplasm of the posterior pituitary0TRAF7 CL E G H8423120456ORPHA:2495MeningiomaHP:0040284 - Very rare
HP:0011752HP:0011754Pituicytoma1 CL E G H


Genes (11) :AKT1 BAP1 NF2 PDGFB PIK3CA SMARCB1 SMARCE1 SMO SUFU TERT TRAF7

Diseases (1) :ORPHA:2495
 

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