Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Encephalopathy (HP:0001298)help
..Starting node
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Recurrent encephalopathy (HP:0007335)help
Term ID: 7335
Name: Recurrent encephalopathy
Synonym: Recurrent cerebellar and extrapyramidal encephalopathy
Definition: Recurrent episodes of brain dysfunction that may be triggered by factors such as metabolic disturbances or infections.
Comments:
Reference: HP:0007335
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute encephalopathy (HP:0006846) help
..expandCongenital encephalopathy (HP:0007239) help
..expandEpileptic encephalopathy (HP:0200134) help
..expandHepatic encephalopathy (HP:0002480) help
..expandHypoglycemic encephalopathy (HP:0006929) help
..expandInfantile encephalopathy (HP:0007105) help
..expandMitochondrial encephalopathy (HP:0006789) help
..expandNecrotizing encephalopathy (HP:0006976) help
..expandNonprogressive encephalopathy (HP:0007030) help
..expandProgressive encephalopathy (HP:0002448) 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:0007335HP:0007335Recurrent encephalopathy0CPT1A CL E G H13742328OMIM:255120Carnitine palmitoyltransferase I deficiency.99


Genes (1) :CPT1A

Diseases (1) :OMIM:255120
 

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