Human Phenotype Ontology 
Grandparent Node:
expandAbnormal uridine diphosphate glucose-4-epimerase level (HP:0410192)help
Parent Node:
expandAbnormal uridine diphosphate glucose-4-epimerase level in red blood cells (HP:0410196)help
..Starting node
..expandDecreased uridine diphosphate glucose-4-epimerase level in red blood cells (HP:0410198)help
Term ID: 410198
Name: Decreased uridine diphosphate glucose-4-epimerase level in red blood cells
Synonym: Decreased UDP-glucose 4-epimerase level in RBCs; Decreased UDP-glucose 4-epimerase level in red blood cells
Definition: A decrease in uridine diphosphate glucose-4-epimerase level in red blood cells. Uridine diphosphate glucose-4-epimerase catalyzes the reaction: UDP-glucose = UDP-galactose.
Comments:
Reference: HP:0410198
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIncreased uridine diphosphate glucose-4-epimerase level in red blood cells (HP:0410197) 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:0410198HP:0410198Decreased uridine diphosphate glucose-4-epimerase level in red blood cells0 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.