Human Phenotype Ontology 
Grandparent Node:
expandAbnormal renal medulla morphology (HP:0100957)help
Parent Node:
expandAbnormality of medullary pyramid morphology (HP:0025361)help
..Starting node
..expandRenal medullary pyramid hypoplasia (HP:0025362)help
Term ID: 25362
Name: Renal medullary pyramid hypoplasia
Synonym: Hypoplasia of the medullary pyramids
Definition: Undergrowth of the pyramid of the adult kidney, cone-shaped structures with a broad base adjacent to the renal cortex and the narrow apex that is termed papilla.
Comments:
Reference: HP:0025362
Genes and Diseases:
 
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 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025362HP:0025362Renal medullary pyramid hypoplasia0 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 December 15 2022 release.