Human Phenotype Ontology 
Grandparent Node:
expandAbnormal renal morphology (HP:0012210)help
Parent Node:
expandNephrocalcinosis (HP:0000121)help
..Starting node
..expandCortical nephrocalcinosis (HP:0012409)help
Term ID: 12409
Name: Cortical nephrocalcinosis
Synonym:
Definition: The deposition of calcium salts in the parenchyma of the renal cortex (the outer portion of the kidney between the renal capsule and the renal medulla).
Comments:
Reference: HP:0012409
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMedullary nephrocalcinosis (HP:0012408) help
..expandMicroscopic nephrocalcinosis (HP:0008327) 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:0012409HP:0012409Cortical nephrocalcinosis0ABCC6 CL E G H36857ORPHA:51608Generalized arterial calcification of infancyHP:0040283 - Occasional415
HP:0012409HP:0012409Cortical nephrocalcinosis0ENPP1 CL E G H51673356ORPHA:51608Generalized arterial calcification of infancyHP:0040283 - Occasional151


Genes (2) :ABCC6 ENPP1

Diseases (1) :ORPHA:51608
 

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