MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Glucose Metabolism Disorders

(UMLS:C1257958)

Definition:: Pathological conditions in which the BLOOD GLUCOSE cannot be maintained within the normal range, such as in HYPOGLYCEMIA and HYPERGLYCEMIA. Etiology of these disorders varies. Plasma glucose concentration is critical to survival for it is the predominant fuel for the CENTRAL NERVOUS SYSTEM.
UMLS ID:: C1257958
MeSH ID:: D044882

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.394

Synonym(s)

Glucose Metabolism Disorders

Disorder of Glucose Metabolism

Disorder of glucose metabolism

Glucose Metabolism Disorder

disorders glucose metabolism

disorders of glucose metabolism

glucose metabolism disorders

metabolic glucose disorders

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Alcohols	23907025 25456265	CTD
2	Bezafibrate	17002798 18230960 20404010	CTD
3	Cadmium Compounds	25043455	CTD
4	Chlorpropamide	16273134	CTD
5	Clozapine	14754788	CTD
6	Dichlorodiphenyl Dichloroethylene	21364465	CTD
7	Gatifloxacin	20397737 23200776	CTD
8	Glipizide	17462097	CTD
9	Lithium Carbonate	5506046	CTD
10	Methotrexate	3789673	CTD
11	Nicotine	18852877	CTD
12	Pentamidine	7481974	CTD
13	Picrotoxin	25456265	CTD
14	Polychlorinated Biphenyls	21364465	CTD
15	Troglitazone	9589670 10726906	CTD
16	bisphenol A	23493373	CTD
17	gamma-Aminobutyric Acid	25456265	CTD
18	rosiglitazone-metformin combination	17462097	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Acid-Base Imbalance	42.9%
2	Calcium Metabolism Disorders	42.9%
3	Iron Metabolism Disorders	42.9%
4	Phosphorus Metabolism Disorders	42.9%
5	Water-Electrolyte Imbalance	42.9%
6	Lipid Metabolism Disorders	42.9%
7	Mitochondrial Diseases	42.9%
8	Hypercalcemia	40.9%
9	Hypocalcemia	40.9%
10	Milk-Alkali Syndrome	40.9%
11	Wasting Syndrome	38.1%
12	Acidosis	31%
13	Alkalosis	31%
14	Amyloidosis	31%
15	Calcinosis	31%
16	Hyperkalemia	31%
17	Hypernatremia	31%
18	Hypokalemia	31%
19	Hyponatremia	31%
20	Xanthomatosis	31%
21	Hypophosphatemia	31%
22	Metabolic acidosis	31%
23	Dyslipidemias	31%
24	Iron Overload	31%
25	Xanthoma	31%
26	Lipodystrophy	30.5%
27	Osteopenia	28.6%
28	Pseudohypoparathyroidism	28.3%
29	Brain Diseases, Metabolic	27.9%
30	Rickets	26.9%
31	Hyperlipoproteinemia Type IV	26.4%
32	Hyperlipoproteinemia Type V	26.4%
33	Acidosis, Lactic	25.4%
34	Calciphylaxis	25.4%
35	Hemosiderosis	25.4%
36	Ketosis	25.4%
37	Ketonuria	25.4%
38	Ketoacidosis	25.4%
39	Ketonemia	25.4%
40	Vascular calcification	25.4%
41	Leigh Disease	25.1%
42	Hypolipoproteinemias	24.8%
43	Hyperhomocysteinemia	24.5%
44	Brain Diseases, Metabolic, Inborn	24.2%
45	Carbamoyl-Phosphate Synthase I Deficiency Disease	23.7%
46	Hyperlipidemia, Familial Combined	23.5%
47	Nutrition Disorders	23.1%
48	Hyperlipoproteinemia Type III	22.8%
49	Hypercholesterolemia	22.7%
50	Hyperlipoproteinemias	22.7%
51	Hypertriglyceridemia	22.7%
52	Osteomalacia	22.3%
53	Hypoalphalipoproteinemias	22%
54	Lactose Intolerance	21.9%
55	Smith-Lemli-Opitz Syndrome	21.1%
56	Galactosemias	21%
57	Urea Cycle Disorders, Inborn	21%
58	Tyrosinemias	21%
59	Dehydration	20.9%
60	Lipomatosis	20.9%
61	Water Intoxication	20.9%
62	Werner Syndrome	20.9%
63	Familial Hypophosphatemic Rickets	20.9%
64	Gaucher Disease	20.6%
65	Achlorhydria	20.5%
66	Amino Acid Metabolism, Inborn Errors	20.5%
67	Bloom Syndrome	20.5%
68	Carbohydrate Metabolism, Inborn Errors	20.5%
69	Metal Metabolism, Inborn Errors	20.5%
70	Osteoporosis	20.5%
71	Progeria	20.5%
72	Lysosomal Storage Diseases	20.5%
73	Bone Demineralization, Pathologic	20.5%
74	Cytochrome-c Oxidase Deficiency	20.5%
75	Peroxisomal Disorders	20.5%
76	Post-Traumatic Osteoporosis	20.5%
77	Celiac Disease	20.2%
78	Sprue, Tropical	20.2%
79	Steatorrhea	20.2%
80	Sprue	20.2%
81	Tay-Sachs Disease	19.4%
82	Glycogen storage disease type II	19.3%
83	Hyperphosphaturia	18.3%
84	Mitochondrial Encephalomyopathies	18.2%
85	Niemann-Pick Disease, Type C	18%
86	Homocystinuria	17.9%
87	Amyloid Neuropathies, Familial	17.2%
88	Acidosis, Respiratory	16.9%
89	Adiposis Dolorosa	16.9%
90	Alkalosis, Respiratory	16.9%
91	Alkaptonuria	16.7%
92	Glycogen Storage Disease	16.7%
93	Hypophosphatasia	16.7%
94	Osteoporosis, Postmenopausal	16.7%
95	Propionic acidemia	16.7%
96	Dihydropyrimidine Dehydrogenase Deficiency	16.7%
97	Cystinosis	16.7%
98	Renal tubular acidosis	16.3%
99	Fabry Disease	15.9%
100	Neuronal Ceroid-Lipofuscinoses	15.7%
101	Mitochondrial Myopathies	15.5%
102	Myelinolysis, Central Pontine	15.4%
103	Reye Syndrome	15.1%
104	Hepatic Encephalopathy	15%
105	Glycogen Storage Disease Type I	14.8%
106	Glycogen Storage Disease Type V	14.8%
107	Mucopolysaccharidosis III	14.6%
108	Child Nutrition Disorders	14.3%
109	Hypervitaminosis A	14.3%
110	Infant Nutrition Disorders	14.3%
111	Malnutrition	14.3%
112	MELAS Syndrome	14.1%
113	HIV-Associated Lipodystrophy Syndrome	14.1%
114	Renal Osteodystrophy	13.9%
115	Renal rickets	13.9%
116	Adrenoleukodystrophy	13.7%
117	Zellweger Syndrome	13.5%
118	Menkes Kinky Hair Syndrome	13.3%
119	HIV Wasting Syndrome	13.3%
120	Nephrocalcinosis	12.5%
121	Tetany	12.5%
122	Hepatolenticular Degeneration	12.4%
123	Porphyrias, Hepatic	12.3%
124	Cerebral Amyloid Angiopathy	12.3%
125	Wernicke Encephalopathy	12.2%
126	Refsum Disease	12.2%
127	Necrobiosis Lipoidica Diabeticorum	12.1%
128	Fanconi Anemia	11.9%
129	Diabetic Ketoacidosis	11.2%
130	Deficiency Diseases	10.3%
131	Starvation	10.3%
132	Refeeding Syndrome	10.3%
133	Familial Periodic Paralysis	10.1%
134	Primary amyloidosis	10.1%
135	Variegate Porphyria	9.9%
136	Acute intermittent porphyria	9.9%
137	Porphyria Cutanea Tarda	9.9%
138	Friedreich Ataxia	9.9%
139	Renal Aminoacidurias	9.8%
140	Fanconi Syndrome	9.8%
141	Pseudohypoaldosteronism	9.8%
142	Liddle Syndrome	9.8%
143	Canavan Disease	9.8%
144	Alexander Disease	9.8%
145	Mucopolysaccharidosis II	9.7%
146	Sjogren-Larsson Syndrome	9.3%
147	Kearns-Sayre syndrome	9.3%
148	Hypokalemic periodic paralysis	8.9%
149	Frontotemporal dementia	8.8%
150	Cystinuria	8.8%
151	Kernicterus	8.7%
152	Cockayne Syndrome	8.6%
153	Kwashiorkor	8.5%
154	Magnesium Deficiency	8.5%
155	Potassium Deficiency	8.5%
156	Protein Deficiency	8.5%
157	Avitaminosis	8.5%
158	Gout	8.4%
159	Amyotrophic Lateral Sclerosis	8.4%
160	Antley-Bixler Syndrome Phenotype	8.2%
161	Ataxia Telangiectasia	7.6%
162	Ascorbic Acid Deficiency	7.6%
163	Vitamin A Deficiency	7.6%
164	Vitamin D Deficiency	7.6%
165	Vitamin E Deficiency	7.6%
166	Marasmus	7.6%
167	Optic Atrophy, Hereditary, Leber	7.4%
168	Arthritis, Gouty	7.4%
169	Folic Acid Deficiency	7.1%
170	Pellagra	7.1%
171	Thiamine Deficiency	7.1%
172	Vitamin B 12 Deficiency	7.1%
173	Vitamin B 6 Deficiency	7.1%
174	Pyridoxine Deficiency	7.1%
175	CREST Syndrome	7%
176	Beriberi	6.9%
177	Xeroderma Pigmentosum	6.8%
178	Albinism	6.3%
179	Glycosuria, Renal	6.1%
180	Ichthyosis, X-Linked	5%
181	Anemia, Pernicious	4.5%
182	Obesity, Abdominal	4.1%
183	Obesity	3.9%
184	Vitamin K Deficiency	3.8%
185	Scurvy	3.5%
186	Pediatric Obesity	3.2%
187	Prader-Willi Syndrome	2.8%
188	Subacute Combined Degeneration	2.3%

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