Hypoglycemia

Symptom Information:

Symptom ID: HPO:0001943
Synonyms:
Hypoglycaemia [HPO:0001943]
Hypoglycemic disorder (disorder) [Orphanet:41720]
Hypoglycemic syndrome (disorder) [Orphanet:41720]
Hypoglycemia (disorder) [Orphanet:41720]
Hypoglycemia [Orphanet:41720]
Hypoglycemia [OMIM:Hypoglycemia]
Hypoglycaemia [Orphanet:41720]
Hypoglycaemia [MedDRA:10020993]
Hypoglycaemia night [MedDRA:10020993]
Hypoglycaemia NOS [MedDRA:10020993]
Hypoglycaemia, unspecified [MedDRA:10020993]
Hypoglycaemic attack [MedDRA:10020993]
Hypoglycaemic reaction [MedDRA:10020993]
Hypoglycemia [MedDRA:10020993]
Hypoglycemia, unspecified [MedDRA:10020993]
Hypoglycemic reaction [MedDRA:10020993]
Hypos [MedDRA:10020993]
Insulin hypoglycaemia [MedDRA:10020993]
Insulin hypoglycemia [MedDRA:10020993]
Other specified hypoglycemia [MedDRA:10020993]
Protoracted hypoglycaemia [MedDRA:10020993]
Reaction hypoglycemic [MedDRA:10020993]
Hypoglycaemia aggravated [MedDRA:10020993]
Hypoglycemic episode [MedDRA:10020993]
Hypoglycemia aggravated [MedDRA:10020993]
Ketotic hypoglycaemia [MedDRA:10020993]
Ketotic hypoglycemia [MedDRA:10020993]
Postprandial hypoglycaemia [MedDRA:10020993]
Postprandial hypoglycemia [MedDRA:10020993]
Hypoglycaemic episode [MedDRA:10020993]
Reaction hypoglycaemic [MedDRA:10020993]
Hypoglycemia night [MedDRA:10020993]
Hypoglycemic attack [MedDRA:10020993]
Asymptomatic hypoglycemia [MedDRA:10020993]
Asymptomatic hypoglycaemia [MedDRA:10020993]
Hypoglycemia (neonatal) [OMIM:Hypoglycemia (neonatal)]
Hypoglycemia, postprandial [OMIM:Hypoglycemia, postprandial]
Quality:
Cross references:
Orphanet:41720 "Hypoglycemia" [Orphanet:41720]
OMIM: "Hypoglycemia" [OMIM:Hypoglycemia]
OMIM: "Hypoglycemia (neonatal)" [OMIM:Hypoglycemia (neonatal)]
OMIM: "Hypoglycemia, postprandial" [OMIM:Hypoglycemia, postprandial]
UMLS:C0020615 "Hypoglycemia" [HPO:0001943]
UMLS:C0020615 "Hypoglycemia" [Orphanet:41720]
Is a (Direct Parents):
MedDRA Hypoglycaemic conditions NEC
HPO         Abnormality of blood glucose concentration
HPO         Ketotic hypoglycemia
Orphanet Anomaly of pancreatic hormones
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)
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)