ONTOLOGY REPORT - ANNOTATIONS
Term: Hypoglycemia
Accession: RDO:0000805
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Definition: A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH.
Synonyms: exact_synonym: Fasting Hypoglycemia; Postabsorptive Hypoglycemia; Postprandial Hypoglycemia; Reactive Hypoglycemia
primary_id: MESH:D007003
alt_id: OMIM:229700 ; OMIM:261650 ; OMIM:261680
Hypoglycemia
G
Abcc8
ATP-binding cassette, subfamily C (CFTR/MRP), member 8
IED
1
96,622,574
96,703,723
RGD:704366
RGD
G
Abcc8
ATP-binding cassette, subfamily C (CFTR/MRP), member 8
IPM
1
96,622,574
96,703,723
RGD:2301896
RGD
G
Acadl
acyl-CoA dehydrogenase, long chain
ISS
9
65,613,130
65,651,775
RGD:704409
RGD
G
Agtr2
angiotensin II receptor, type 2
ISS
RGD:2313551
RGD
G
Cebpb
CCAAT/enhancer binding protein (C/EBP), beta
ISS
3
158,826,021
158,827,848
RGD:1300293
RGD
G
Crh
corticotropin releasing hormone
IED
2
104,764,023
104,765,887
RGD:704397
RGD
G
Epo
erythropoietin
ISS
12
19,551,768
19,555,208
RGD:2313835
RGD
G
Fbp1
fructose-1,6-bisphosphatase 1
ISS
17
7,795,717
7,818,041
RGD:7240710
OMIM
G
Gck
glucokinase
ISS
14
86,572,518
86,587,723
RGD:1601294
RGD
G
Glud1
glutamate dehydrogenase 1
ISS
16
9,965,718
9,999,254
RGD:1601353
RGD
G
Grin2b
glutamate receptor, ionotropic, N-methyl D-aspartate 2B
IEP
4
172,721,895
173,183,187
RGD:4107025
RGD
G
Hadh
hydroxyacyl-CoA dehydrogenase
ISS
2
228,698,545
228,751,691
RGD:2306664
RGD
G
Hnf4a
hepatocyte nuclear factor 4, alpha
ISS
3
154,459,863
154,482,825
RGD:2301837
RGD
G
Inppl1
inositol polyphosphate phosphatase-like 1
ISS
1
159,278,131
159,292,740
RGD:737755
RGD
G
Pck1
phosphoenolpyruvate carboxykinase 1 (soluble)
ISS
3
164,012,410
164,018,359
RGD:7240710
OMIM
G
Pck2
phosphoenolpyruvate carboxykinase 2 (mitochondrial)
ISS
15
33,671,834
33,680,613
RGD:7240710
OMIM
G
Pik3r1
phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
ISS
2
32,602,673
32,675,350
RGD:737788
RGD
G
Pla2g1b
phospholipase A2, group IB, pancreas
ISS
12
42,405,475
42,415,189
RGD:1302550
RGD
G
Pnmt
phenylethanolamine-N-methyltransferase
IEP
RGD:5130725
RGD
G
Ppp1r3a
protein phosphatase 1, regulatory subunit 3A
ISS
4
40,195,325
40,235,913
RGD:1601469
RGD
G
Prl
prolactin
ISS
17
44,699,101
44,709,162
RGD:1642557
RGD
G
Th
tyrosine hydroxylase
IEP
1
203,164,253
203,171,506
RGD:5130724
RGD
G
Ucp3
uncoupling protein 3 (mitochondrial, proton carrier)
ISS
1
157,896,001
157,909,608
RGD:737762
RGD
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
G
Hmgcs2
3-hydroxy-3-methylglutaryl-CoA synthase 2 (mitochondrial)
ISS
2
193,128,736
193,143,106
RGD:7240710
OMIM
ACTH Deficiency, Isolated
G
Tbx19
T-box 19
ISS
13
80,890,762
80,913,604
RGD:7240710
OMIM
Carnitine palmitoyl transferase 1A deficiency
G
Cpt1a
carnitine palmitoyltransferase 1a, liver
ISS
1
205,852,800
205,912,972
RGD:7240710
OMIM
Carnitine Palmitoyltransferase II Deficiency, Infantile
G
Cpt2
carnitine palmitoyltransferase 2
ISS
5
129,007,685
129,025,501
RGD:7240710
OMIM
Hyperinsulinemic hypoglycemia, familial, 1
G
Abcc8
ATP-binding cassette, subfamily C (CFTR/MRP), member 8
ISS
1
96,622,574
96,703,723
RGD:7240710
OMIM
Hyperinsulinemic hypoglycemia, familial, 2
G
Kcnj11
potassium inwardly rectifying channel, subfamily J, member 11
ISS
1
96,614,960
96,617,993
RGD:7240710
OMIM
Hyperinsulinemic hypoglycemia, familial, 3
G
Gck
glucokinase
ISS
14
86,572,518
86,587,723
RGD:7240710
OMIM
Hyperinsulinemic Hypoglycemia, Familial, 5
G
Insr
insulin receptor
ISS
12
2,934,967
3,087,691
RGD:7240710
OMIM
Hyperinsulinemic hypoglycemia, familial, 6
G
Glud1
glutamate dehydrogenase 1
ISS
16
9,965,718
9,999,254
RGD:7240710
OMIM
Hyperinsulinemic hypoglycemia, familial, 7
G
Slc16a1
solute carrier family 16, member 1 (monocarboxylic acid transporter 1)
ISS
2
199,860,341
199,879,856
RGD:7240710
OMIM
Hypoglycemia, leucine-induced
G
Abcc8
ATP-binding cassette, subfamily C (CFTR/MRP), member 8
ISS
1
96,622,574
96,703,723
RGD:7240710
OMIM
Term paths to the root one longest all shortest one shortest all one shortest and longest all longest
Path 1
Diseases
30711
Nutritional and Metabolic Diseases
5312
Metabolic Diseases
4690
Glucose Metabolism Disorders
2836
Hypoglycemia
34
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
1
ACTH Deficiency, Isolated
1
Carnitine Palmitoyltransferase I Deficiency
0
Carnitine Palmitoyltransferase II Deficiency, Infantile
1
Carnitine palmitoyl transferase 1A deficiency
1
Congenital Hyperinsulinism +
2
Hyperinsulinemic Hypoglycemia, Familial, 4
0
Hyperinsulinemic Hypoglycemia, Familial, 5
1
Hyperinsulinemic hypoglycemia, familial, 3
1
Hyperinsulinemic hypoglycemia, familial, 6
1
Hyperinsulinemic hypoglycemia, familial, 7
1
Hypoglycemia, Neonatal, Simulating Foetopathia Diabetica
0
Hypoglycemia, leucine-induced
1
Insulin Coma
0