Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of digestive system physiology (HP:0025032)help
Parent Node:
expand
Abnormality of hepatobiliary system physiology (HP:0025155)help
..Starting node
..expand
Reye syndrome-like episodes (HP:0006582)help
Term ID: 6582
Name: Reye syndrome-like episodes
Synonym:
Definition: Repeated occurrences of acute noninflammatory encephalopathy and fatty degenerative liver failure.
Comments:
Reference: HP:0006582
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDecreased liver function (HP:0001410) help
..expandDecreased mitochondrial complex III activity in liver tissue (HP:0006558) 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:0006582HP:0006582Reye syndrome-like episodes0FBP1 CL E G H22033606ORPHA:348Fructose-1,6-bisphosphatase deficiencyHP:0040283 - Occasional64
HP:0006582HP:0006582Reye syndrome-like episodes0HMGCL CL E G H31555005ORPHA:203-hydroxy-3-methylglutaric aciduriaHP:0040282 - Frequent35
HP:0006582HP:0006582Reye syndrome-like episodes0MPV17 CL E G H43587224OMIM:256810Navajo neurohepatopathy.56
HP:0006582HP:0006582Reye syndrome-like episodes0NAGS CL E G H16241717996ORPHA:927Hyperammonemia due to N-acetylglutamate synthase deficiencyHP:0040284 - Very rare36


Genes (4) :FBP1 HMGCL MPV17 NAGS

Diseases (4) :ORPHA:348 ORPHA:20 OMIM:256810 ORPHA:927
 

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