modern wellness · Symptom
Hypoglycemia
🩺 HPO Source
HPO ID
HPO Label
Hypoglycemia
HPO Definition
A decreased concentration of glucose in the blood.
🔤 Synonyms (2)
Synonyms
HypoglycaemiaLow blood sugar
🔗 Cross-References (4)
SNOMEDCT_US237630007
SNOMEDCT_US271327008
SNOMEDCT_US302866003
UMLSC0020615
🔼 Broader Terms (1)
HP:0011015Abnormal blood glucose concentration
🏥 Conditions where Hypoglycemia appears
40 · bridged via HPO ↔ OMIM
phenotype OMIM 300438
2-Methyl-3-Hydroxybutyric Aciduria
ev: IEA
syndrome OMIM 610006
2-Methylbutyryl-Coa Dehydrogenase Deficiency
ev: IEA
syndrome OMIM 605911
3-Hydroxy-3-Methylglutaryl-Coa Synthase 2 Deficiency
freq: 25/28 ev: PCS
syndrome OMIM 210200
3-Methylcrotonyl Coa Carboxylase 1 Deficiency
ev: TAS
syndrome OMIM 210210
3-Methylcrotonyl Coa Carboxylase 2 Deficiency
ev: IEA
syndrome OMIM 614739
3-Methylglutaconic Aciduria With Deafness, Encephalopathy, And Leigh-Like Syndrome
ev: TAS
syndrome OMIM 611126
Acyl-Coa Dehydrogenase Family, Member 9, Deficiency Of
ev: IEA
syndrome OMIM 240200
Addison Disease
ev: IEA
phenotype OMIM 240200
Adrenal Hypoplasia
ev: IEA
syndrome OMIM 608688
Aicar Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
freq: 1/1 ev: PCS
disease OMIM 236100
Alobar Holoprosencephaly
ev: IEA
syndrome OMIM 201750
Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis
freq: 1/3 ev: PCS
disease OMIM 236100
Arhinencephaly
ev: IEA
syndrome OMIM 613658
Brain Calcification Rajab Type
freq: 1/1 ev: PCS
syndrome OMIM 615751
Carbonic Anhydrase Va Deficiency, Hyperammonemia Due To
freq: 4/4 ev: PCS
syndrome OMIM 608836
Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal
freq: 1/2 ev: PCS
syndrome OMIM 212138
Carnitine-Acylcarnitine Translocase Deficiency
ev: IEA
syndrome OMIM 616007
Cataracts, Growth Hormone Deficiency, Sensory Neuropathy, Sensorineural Hearing Loss, And Skeletal Dysplasia
freq: 3/3 ev: PCS
syndrome OMIM 617049
Cholestasis, Progressive Familial Intrahepatic, 5
freq: 3/4 ev: PCS
syndrome OMIM 248600
Classic Maple Syrup Urine Disease
ev: IEA
syndrome OMIM 614702
Combined Oxidative Phosphorylation Deficiency 10
freq: 1/3 ev: PCS
syndrome OMIM 617872
Combined Oxidative Phosphorylation Deficiency 34
freq: 2/2 ev: PCS
syndrome OMIM 617950
Combined Oxidative Phosphorylation Deficiency 36
freq: 2/2 ev: PCS
disease OMIM 240200
Congenital Absence of Adrenal Gland
ev: IEA
disease OMIM 201910
Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency
ev: IEA
syndrome OMIM 607143
Congenital Disorder of Glycosylation Type 1G
freq: 1/1 ev: PCS
syndrome OMIM 608779
Congenital Disorder of Glycosylation Type 2E
freq: 1/3 ev: PCS
syndrome OMIM 618005
Congenital Disorder of Glycosylation With Defective Fucosylation
freq: 1/3 ev: PCS
syndrome OMIM 218040
Costello Syndrome (Disorder)
ev: IEA
disease OMIM 236100
Cyclocephaly
ev: IEA
syndrome OMIM 220120
D-Glyceric Aciduria
freq: 1/3 ev: PCS
syndrome OMIM 220120
D-Glycericacidemia
freq: 1/3 ev: PCS
syndrome OMIM 307030
Deficiency of Glycerol Kinase
ev: TAS
syndrome OMIM 607398
Familial Glucocorticoid Deficiency Type 2
freq: 1/1 ev: PCS
syndrome OMIM 616026
Fanconi Renotubular Syndrome 4 With Maturity-Onset Diabetes of The Young
freq: 1/1 onset: HP:0003623 ev: PCS
syndrome OMIM 229700
Fructose-1,6-Diphosphatase Deficiency
freq: 1/1 ev: PCS
syndrome OMIM 614736
Glucocorticoid Deficiency 4 With Or Without Mineralocorticoid Deficiency
ev: TAS
syndrome OMIM 615962
Glucocorticoid Receptor Deficiency
ev: TAS
syndrome OMIM 232220
Glucose-6-Phosphate Transport Defect
ev: IEA
syndrome OMIM 231680
Glutaric Acidemia Iia
ev: IEA