Hypoglycemia
Symptom Information:
Symptom ID: | HPO:0001943 | |||||||||||||||||||||||||||||||||||||
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) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Glucose metabolism disorders (incl diabetes mellitus)(MedDRA:10018424) Hypoglycaemic conditions NEC(MedDRA:10021001) Hypoglycemia(HPO:0001943) |
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Database Frequency: | 131 / 7739 | |||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
2-methylbutyryl-CoA dehydrogenase deficiency | (Orphanet:79157) |
2p21 microdeletion syndrome | (Orphanet:163693) |
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY | (OMIM:231530) |
3-hydroxy-3-methylglutaric aciduria | (Orphanet:20) |
3-hydroxy-3-methylglutaryl-CoA synthase deficiency | (Orphanet:35701) |
3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency | (Orphanet:276580) |
Autosomal dominant hyperinsulinism due to SUR1 deficiency | (Orphanet:276575) |
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency | (Orphanet:79644) |
Autosomal recessive hyperinsulinism due to SUR1 deficiency | (Orphanet:79643) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Barth syndrome | (Orphanet:111) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
CADASIL | (Orphanet:136) |
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO | (OMIM:615751) |
CORTICOTROPIN-RELEASING HORMONE | (OMIM:122560) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine palmitoyl transferase II deficiency | (Orphanet:157) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Cholera | (Orphanet:173) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
Classic galactosemia | (Orphanet:79239) |
Classic maple syrup urine disease | (Orphanet:268145) |
Congenital disorder of glycosylation | (Orphanet:137) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Costello syndrome | (Orphanet:3071) |
Cytomegalic congenital adrenal hypoplasia | (Orphanet:95702) |
DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE | (OMIM:223500) |
Diabetic embryopathy | (Orphanet:1926) |
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency | (Orphanet:276603) |
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency | (Orphanet:276598) |
Endomyocardial fibroelastosis | (Orphanet:2022) |
Exercise-induced hyperinsulinism | (Orphanet:165991) |
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG | (OMIM:616026) |
FRUCTOSE AND GALACTOSE INTOLERANCE | (OMIM:229500) |
Fatal infantile lactic acidosis with methylmalonic aciduria | (Orphanet:17) |
Fructose-1,6-bisphosphatase deficiency | (Orphanet:348) |
GLUCOCORTICOID DEFICIENCY 1 | (OMIM:202200) |
GLUCOCORTICOID DEFICIENCY 2 | (OMIM:607398) |
GLUCOCORTICOID DEFICIENCY 3 | (OMIM:609197) |
GLUCOCORTICOID DEFICIENCY 4 | (OMIM:614736) |
GLUCOCORTICOID RESISTANCE, GENERALIZED | (OMIM:615962) |
GLYCOGEN STORAGE DISEASE Ic | (OMIM:232240) |
GRACILE syndrome | (Orphanet:53693) |
Galactosemia | (Orphanet:352) |
Gaucher disease type 2 | (Orphanet:77260) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
Glycogen storage disease due to liver glycogen phosphorylase deficiency | (Orphanet:369) |
Glycogen storage disease due to liver phosphorylase kinase deficiency | (Orphanet:264580) |
Glycogen storage disease due to phosphorylase kinase deficiency | (Orphanet:370) |
Growth hormone insensitivity syndrome | (Orphanet:181393) |
HOLOPROSENCEPHALY 1 | (OMIM:236100) |
HOMOZYGOUS 11p15-p14 DELETION SYNDROME | (OMIM:606528) |
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4 | (OMIM:609975) |
HYPOADRENOCORTICISM, FAMILIAL | (OMIM:240200) |
HYPOGLYCEMIA, LEUCINE-INDUCED | (OMIM:240800) |
Hereditary fructose intolerance | (Orphanet:469) |
Histidinuria - renal tubular defect | (Orphanet:2158) |
Holoprosencephaly | (Orphanet:2162) |
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | (Orphanet:401948) |
Hyperinsulinism due to INSR deficiency | (Orphanet:263458) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Isolated growth hormone deficiency type IA | (Orphanet:231662) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
Kallmann syndrome - heart disease | (Orphanet:2326) |
Laron syndrome | (Orphanet:633) |
Leprechaunism | (Orphanet:508) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
MEGDEL syndrome | (Orphanet:352328) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3 | (OMIM:615158) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5 | (OMIM:615160) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9 | (OMIM:616111) |
MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY | (OMIM:614741) |
MPI-CDG | (Orphanet:79319) |
Malonic aciduria | (Orphanet:943) |
Medium chain acyl-CoA dehydrogenase deficiency | (Orphanet:42) |
Menkes disease | (Orphanet:565) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | (Orphanet:314637) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal hemochromatosis | (Orphanet:446) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PGM1-CDG | (Orphanet:319646) |
Phosphoenolpyruvate carboxykinase 1 deficiency | (Orphanet:79316) |
Phosphoenolpyruvate carboxykinase 2 deficiency | (Orphanet:79317) |
Phosphoenolpyruvate carboxykinase deficiency | (Orphanet:2880) |
Pituitary stalk interruption syndrome | (Orphanet:95496) |
Propionic acidemia | (Orphanet:35) |
Pyridoxal phosphate-responsive seizures | (Orphanet:79096) |
Pyruvate carboxylase deficiency | (Orphanet:3008) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
Pyruvate dehydrogenase phosphatase deficiency | (Orphanet:79246) |
RIBOFLAVIN DEFICIENCY | (OMIM:615026) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:35123) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Short stature - pituitary and cerebellar defects - small sella turcica | (Orphanet:85442) |
Silver-Russell syndrome | (Orphanet:813) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Sotos syndrome | (Orphanet:821) |
TENORIO SYNDROME | (OMIM:616260) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |
Timothy syndrome | (Orphanet:65283) |
Tyrosinemia type 1 | (Orphanet:882) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |