Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of acid-base homeostasis (HP:0004360)help
Parent Node:
expandAcidosis (HP:0001941)help
..Starting node
..expandPhenylpyruvic acidemia (HP:0004920)help
Term ID: 4920
Name: Phenylpyruvic acidemia
Synonym:
Definition:
Comments:
Reference: HP:0004920
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandChronic acidosis (HP:0012468) help
..expandDicarboxylic acidemia (HP:0040145) help
..expandElevated circulating glutaric acid concentration (HP:0003530) help
..expandHyperchloremic acidosis (HP:0001995) help
..expandIncreased serum lactate (HP:0002151) help
..expandKetoacidosis (HP:0001993) help
..expandLactic acidosis (HP:0003128) help
..expandMetabolic acidosis (HP:0001942) help
..expandMethylmalonic acidemia (HP:0002912) help
..expandOroticaciduria (HP:0003218) help
..expandPropionic acidemia (HP:0003571) help
..expandRenal tubular acidosis (HP:0001947) help
..expandRespiratory acidosis (HP:0005972) 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:0004920HP:0004920Phenylpyruvic acidemia0 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.