modern wellness · Symptom
Hyperglycemia
🩺 HPO Source
HPO ID
HPO Label
Hyperglycemia
HPO Definition
An increased concentration of glucose in the blood.
🔤 Synonyms (2)
Synonyms
High blood glucoseHigh blood sugar
🔗 Cross-References (3)
SNOMEDCT_US237598005
SNOMEDCT_US80394007
UMLSC0020456
🔼 Broader Terms (1)
HP:0011015Abnormal blood glucose concentration
🏥 Conditions where Hyperglycemia appears
37 · bridged via HPO ↔ OMIM
syndrome OMIM 615812
Abdominal Obesity-Metabolic Syndrome 3
freq: 5/27 ev: PCS
syndrome OMIM 615954
Acth-Independent Macronodular Adrenal Hyperplasia 2
ev: TAS
syndrome OMIM 203800
Alstrom Syndrome
freq: 1/1 ev: PCS
syndrome OMIM 615986
Bardet-Biedl Syndrome 9
freq: 1/1 ev: PCS
syndrome OMIM 615522
Cole Disease
freq: 0/4 ev: PCS
syndrome OMIM 606176
Developmental Delay, Epilepsy, And Neonatal Diabetes
ev: PCS
syndrome OMIM 222100
Diabetes Mellitus, Insulin-Dependent
ev: IEA
syndrome OMIM 606176
Diabetes Mellitus, Permanent Neonatal
ev: PCS
syndrome OMIM 601410
Diabetes Mellitus, Transient Neonatal, 1
ev: IEA
syndrome OMIM 610582
Diabetes Mellitus, Transient Neonatal, 3 (Disorder)
freq: 4/4 ev: PCS
syndrome OMIM 520000
Diabetes-Deafness Syndrome Maternally Transmitted (Disorder)
ev: IEA
syndrome OMIM 610370
Diarrhea 4, Malabsorptive, Congenital
freq: 2/3 ev: PCS
syndrome OMIM 246200
Donohue Syndrome
ev: IEA
syndrome OMIM 608600
Familial Partial Lipodystrophy, Type 1
ev: IEA
syndrome OMIM 151660
Familial Partial Lipodystrophy, Type 2
freq: 8/9 ev: PCS
syndrome OMIM 604367
Familial Partial Lipodystrophy, Type 3
freq: 2/3 ev: PCS
disease OMIM 175700
Greig Cephalopolysyndactyly Syndrome
freq: HP:0040283 ev: PCS
syndrome OMIM 600001
Heart Defects, Congenital, And Other Congenital Anomalies
ev: TAS
syndrome OMIM 616214
Hyperproinsulinemia
freq: HP:0040283 ev: TAS
syndrome OMIM 246200
Insulin Receptor, Defect In
ev: IEA
syndrome OMIM 220111
Leigh Syndrome , French Canadian Type
ev: TAS
syndrome OMIM 248370
Mandibuloacral Dysostosis
freq: 0/9 ev: PCS
syndrome OMIM 608612
Mandibuloacral Dysplasia With Type B Lipodystrophy
ev: IEA
syndrome OMIM 613370
Maturity-Onset Diabetes of The Young, Type 10
onset: HP:0003593 ev: PCS
syndrome OMIM 616329
Maturity-Onset Diabetes of The Young, Type 13
freq: 1/4 ev: PCS
syndrome OMIM 600496
Maturity-Onset Diabetes of The Young, Type 3 (Disorder)
ev: IEA
syndrome OMIM 609812
Maturity-Onset Diabetes of The Young, Type 8, With Exocrine Dysfunction
ev: PCS
syndrome OMIM 612225
Maturity-Onset Diabetes of The Young, Type 9 (Disorder)
freq: 1/1 ev: PCS
syndrome OMIM 615710
Mitchell-Riley Syndrome
ev: TAS
syndrome OMIM 124000
Mitochondrial Complex Iii Deficiency, Nuclear Type 1
freq: 1/2 ev: PCS
syndrome OMIM 615453
Mitochondrial Complex Iii Deficiency, Nuclear Type 6
freq: 2/2 ev: PCS
syndrome OMIM 604484
Neuropathy, Hereditary Motor And Sensory, Okinawa Type
freq: 4/13 ev: PCS
syndrome OMIM 600001
Pancreatic Agenesis And Congenital Heart Defects
ev: TAS
syndrome OMIM 609069
Pancreatic And Cerebellar Agenesis
freq: 1/1 ev: PCS
syndrome OMIM 262190
Rabson-Mendenhall Syndrome
ev: IEA
syndrome OMIM 269880
Short Syndrome
ev: IEA
syndrome OMIM 277700
Werner Syndrome
freq: 2/2 ev: PCS