Hypoglycemic seizures

Symptom Information:

Symptom ID: HPO:0002173
Synonyms:
Hypoglycemic seizures [OMIM:Hypoglycemic seizures]
Seizures, hypoglycemic [OMIM:Seizures, hypoglycemic]
Seizures, hypoglycemic (in some patients) [OMIM:Seizures, hypoglycemic (in some patients)]
Hypoglycemic convulsion [IBIS,cm]
Quality:
Cross references:
OMIM: "Hypoglycemic seizures" [OMIM:Hypoglycemic seizures]
OMIM: "Seizures, hypoglycemic" [OMIM:Seizures, hypoglycemic]
OMIM: "Seizures, hypoglycemic (in some patients)" [OMIM:Seizures, hypoglycemic (in some patients)]
Is a (Direct Parents):
HPO         Symptomatic seizures
HPO         Hypoglycemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Seizures(HPO:0001250)
                Symptomatic seizures(HPO:0011145)
                   Hypoglycemic seizures(HPO:0002173)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013)
             Abnormal glucose homeostasis(HPO:0011014)
                Abnormality of blood glucose concentration(HPO:0011015)
                   Hypoglycemia(HPO:0001943)
                      Hypoglycemic seizures(HPO:0002173)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (OMIM:231530)
Autosomal dominant hyperinsulinism due to SUR1 deficiency (Orphanet:276575)
Autosomal recessive hyperinsulinism due to SUR1 deficiency (Orphanet:79643)
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency (Orphanet:276598)
Exercise-induced hyperinsulinism (Orphanet:165991)
GLUCOCORTICOID DEFICIENCY 4 (OMIM:614736)
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4 (OMIM:609975)
HYPOGLYCEMIA, LEUCINE-INDUCED (OMIM:240800)
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (Orphanet:71212)
Hyperinsulinism due to INSR deficiency (Orphanet:263458)
Hyperinsulinism due to glucokinase deficiency (Orphanet:79299)
Hyperinsulinism-hyperammonemia syndrome (Orphanet:35878)
Hypoinsulinemic hypoglycemia and body hemihypertrophy (Orphanet:293964)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Obesity due to pro-opiomelanocortin deficiency (Orphanet:71526)
PITUITARY HORMONE DEFICIENCY, COMBINED, 2 (OMIM:262600)
Panhypopituitarism (Orphanet:90695)
Wolfram syndrome 1 (OMIM:222300)