MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Water-Electrolyte Imbalance

(UMLS:C0043065)

Definition:: Disturbances in the body's WATER-ELECTROLYTE BALANCE.
UMLS ID:: C0043065
MeSH ID:: D014883

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.950

Synonym(s)

Water-Electrolyte Imbalance

Water-electrolyte imbalances

water electrolyte imbalance

water-electrolyte imbalance

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Aspirin	10910377	CTD
2	Calcium Compounds	7696938	CTD
3	Cyclophosphamide	582354	CTD
4	Foscarnet	7802522 8384030	CTD
5	Ganciclovir	7802522	CTD
6	Gentamicins	7182340 8971904	CTD
7	Lithium Carbonate	4751821	CTD
8	Methotrexate	3176582	CTD
9	Potassium	7696938	CTD
10	Prednisone	5025095	CTD
11	Sodium	7696938	CTD
12	Vincristine	582354	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	Lipid Metabolism Disorders	42.9%
6	Mitochondrial Diseases	42.9%
7	Glucose Metabolism Disorders	42.9%
8	Wasting Syndrome	38.1%
9	Acidosis	31%
10	Alkalosis	31%
11	Amyloidosis	31%
12	Calcinosis	31%
13	Hyperglycemia	31%
14	Hyperinsulinism	31%
15	Hypoglycemia	31%
16	Xanthomatosis	31%
17	Hypophosphatemia	31%
18	Metabolic acidosis	31%
19	Dyslipidemias	31%
20	Iron Overload	31%
21	Xanthoma	31%
22	Lipodystrophy	30.5%
23	Osteopenia	28.6%
24	Pseudohypoparathyroidism	28.3%
25	Brain Diseases, Metabolic	27.9%
26	Rickets	26.9%
27	Hyperlipoproteinemia Type IV	26.4%
28	Hyperlipoproteinemia Type V	26.4%
29	Acidosis, Lactic	25.4%
30	Calciphylaxis	25.4%
31	Hemosiderosis	25.4%
32	Ketosis	25.4%
33	Ketonuria	25.4%
34	Ketoacidosis	25.4%
35	Ketonemia	25.4%
36	Vascular calcification	25.4%
37	Leigh Disease	25.1%
38	Hypolipoproteinemias	24.8%
39	Hyperhomocysteinemia	24.5%
40	Brain Diseases, Metabolic, Inborn	24.2%
41	Carbamoyl-Phosphate Synthase I Deficiency Disease	23.7%
42	Diabetic Ketoacidosis	23.7%
43	Hyperlipidemia, Familial Combined	23.5%
44	Nutrition Disorders	23.1%
45	Hyperlipoproteinemia Type III	22.8%
46	Hypercholesterolemia	22.7%
47	Hyperlipoproteinemias	22.7%
48	Hypertriglyceridemia	22.7%
49	Osteomalacia	22.3%
50	Hypoalphalipoproteinemias	22%
51	Diabetes Mellitus	22%
52	Lactose Intolerance	21.9%
53	Smith-Lemli-Opitz Syndrome	21.1%
54	Galactosemias	21%
55	Urea Cycle Disorders, Inborn	21%
56	Tyrosinemias	21%
57	Lipomatosis	20.9%
58	Werner Syndrome	20.9%
59	Familial Hypophosphatemic Rickets	20.9%
60	Gaucher Disease	20.6%
61	Congenital Hyperinsulinism	20.5%
62	Achlorhydria	20.5%
63	Amino Acid Metabolism, Inborn Errors	20.5%
64	Bloom Syndrome	20.5%
65	Carbohydrate Metabolism, Inborn Errors	20.5%
66	Hypercalcemia	20.5%
67	Hypocalcemia	20.5%
68	Metal Metabolism, Inborn Errors	20.5%
69	Milk-Alkali Syndrome	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	Nesidioblastosis	17.9%
87	Homocystinuria	17.9%
88	Amyloid Neuropathies, Familial	17.2%
89	Acidosis, Respiratory	16.9%
90	Adiposis Dolorosa	16.9%
91	Alkalosis, Respiratory	16.9%
92	Alkaptonuria	16.7%
93	Glycogen Storage Disease	16.7%
94	Hypophosphatasia	16.7%
95	Insulin Resistance	16.7%
96	Osteoporosis, Postmenopausal	16.7%
97	Propionic acidemia	16.7%
98	Dihydropyrimidine Dehydrogenase Deficiency	16.7%
99	Cystinosis	16.7%
100	Renal tubular acidosis	16.3%
101	Fabry Disease	15.9%
102	Neuronal Ceroid-Lipofuscinoses	15.7%
103	Mitochondrial Myopathies	15.5%
104	Myelinolysis, Central Pontine	15.4%
105	Glycosuria	15.1%
106	Reye Syndrome	15.1%
107	Hepatic Encephalopathy	15%
108	Glycogen Storage Disease Type I	14.8%
109	Glycogen Storage Disease Type V	14.8%
110	Mucopolysaccharidosis III	14.6%
111	Child Nutrition Disorders	14.3%
112	Hypervitaminosis A	14.3%
113	Infant Nutrition Disorders	14.3%
114	Malnutrition	14.3%
115	MELAS Syndrome	14.1%
116	HIV-Associated Lipodystrophy Syndrome	14.1%
117	Renal Osteodystrophy	13.9%
118	Renal rickets	13.9%
119	Adrenoleukodystrophy	13.7%
120	Zellweger Syndrome	13.5%
121	Menkes Kinky Hair Syndrome	13.3%
122	HIV Wasting Syndrome	13.3%
123	Gestational Diabetes	13%
124	Latent Autoimmune Diabetes in Adults	13%
125	Diabetes Mellitus, Experimental	12.8%
126	Nephrocalcinosis	12.5%
127	Tetany	12.5%
128	Hepatolenticular Degeneration	12.4%
129	Porphyrias, Hepatic	12.3%
130	Cerebral Amyloid Angiopathy	12.3%
131	Wernicke Encephalopathy	12.2%
132	Glycosuria, Renal	12.2%
133	Refsum Disease	12.2%
134	Necrobiosis Lipoidica Diabeticorum	12.1%
135	Fanconi Anemia	11.9%
136	Deficiency Diseases	10.3%
137	Starvation	10.3%
138	Refeeding Syndrome	10.3%
139	Familial Periodic Paralysis	10.1%
140	Primary amyloidosis	10.1%
141	Variegate Porphyria	9.9%
142	Acute intermittent porphyria	9.9%
143	Porphyria Cutanea Tarda	9.9%
144	Friedreich Ataxia	9.9%
145	Renal Aminoacidurias	9.8%
146	Fanconi Syndrome	9.8%
147	Pseudohypoaldosteronism	9.8%
148	Liddle Syndrome	9.8%
149	Canavan Disease	9.8%
150	Alexander Disease	9.8%
151	Mucopolysaccharidosis II	9.7%
152	Sjogren-Larsson Syndrome	9.3%
153	Kearns-Sayre syndrome	9.3%
154	Hypokalemic periodic paralysis	8.9%
155	Frontotemporal dementia	8.8%
156	Cystinuria	8.8%
157	Kernicterus	8.7%
158	Cockayne Syndrome	8.6%
159	Kwashiorkor	8.5%
160	Magnesium Deficiency	8.5%
161	Potassium Deficiency	8.5%
162	Protein Deficiency	8.5%
163	Avitaminosis	8.5%
164	Gout	8.4%
165	Amyotrophic Lateral Sclerosis	8.4%
166	Antley-Bixler Syndrome Phenotype	8.2%
167	Ataxia Telangiectasia	7.6%
168	Ascorbic Acid Deficiency	7.6%
169	Vitamin A Deficiency	7.6%
170	Vitamin D Deficiency	7.6%
171	Vitamin E Deficiency	7.6%
172	Marasmus	7.6%
173	Optic Atrophy, Hereditary, Leber	7.4%
174	Arthritis, Gouty	7.4%
175	Folic Acid Deficiency	7.1%
176	Pellagra	7.1%
177	Thiamine Deficiency	7.1%
178	Vitamin B 12 Deficiency	7.1%
179	Vitamin B 6 Deficiency	7.1%
180	Pyridoxine Deficiency	7.1%
181	CREST Syndrome	7%
182	Beriberi	6.9%
183	Xeroderma Pigmentosum	6.8%
184	Albinism	6.3%
185	Ichthyosis, X-Linked	5%
186	Anemia, Pernicious	4.5%
187	Obesity, Abdominal	4.1%
188	Obesity	3.9%
189	Vitamin K Deficiency	3.8%
190	Scurvy	3.5%
191	Pediatric Obesity	3.2%
192	Prader-Willi Syndrome	2.8%
193	Subacute Combined Degeneration	2.3%

Page last updated at 2020-05-25 10:01:57 (Asia/Shanghai) | You are visitor No. 120234