Hypoglycemic seizures
Symptom Information:
Symptom ID: | HPO:0002173 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) 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) MedDRA: |
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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) |