Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cerebral morphology (HP:0002060)help
Grandparent Node:
expandEctopic calcification (HP:0010766)help
Parent Node:
expandAbnormality of the anterior pituitary (HP:0011747)help
Parent Node:
expandCerebral calcification (HP:0002514)help
..Starting node
..expandPituitary calcification (HP:0010513)help
Term ID: 10513
Name: Pituitary calcification
Synonym:
Definition: Deposition of calcium salts in the pituitary gland.
Comments:
Reference: HP:0010513
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBasal ganglia calcification (HP:0002135) help
..expandBilateral intracerebral calcifications (HP:0005671) help
..expandCalcification of falx cerebri (HP:0005462) help
..expandChoroid plexus calcification (HP:0006960) help
..expandCongenital intracerebral calcification (HP:0006906) help
..expandDiffuse cerebral calcification (HP:0005849) help
..expandIntracerebral periventricular calcifications (HP:0007229) help
..expandMeningeal calcification (HP:0100250) help
..expandMidline brain calcifications (HP:0007045) help
..expandNonarteriosclerotic cerebral calcification (HP:0007238) help
..expandSubcortical white matter calcifications (HP:0007346) 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:0010513HP:0010513Pituitary calcification0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.