Human Phenotype Ontology 
Grandparent Node:
expandAbnormal nervous system physiology (HP:0012638)help
Parent Node:
expandEncephalopathy (HP:0001298)help
..Starting node
..expandHypoglycemic encephalopathy (HP:0006929)help
Term ID: 6929
Name: Hypoglycemic encephalopathy
Synonym:
Definition: Brain damage related to a lowering of blood glucose below a critical level (around 30 mg/dl), which may lead to confusion, lethargy and delirium followed by seizures and coma. Prolonged hypoglycemia may lead to irreversible brain damage.
Comments:
Reference: HP:0006929
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
..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
..expandRecurrent encephalopathy (HP:0007335) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006929HP:0006929Hypoglycemic encephalopathy0HADH CL E G H303371212ORPHA12294799601609
HP:0006929HP:0006929Hypoglycemic encephalopathy0HADH CL E G H3033231530Deficiency of 3-hydroxyacyl-CoA dehydrogenase231530C1291230OMIM12294799601609
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :HADH

Diseases (2) :71212 231530
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.