MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Acid-Base Imbalance

(UMLS:C0001118)

Definition:: Disturbances in the ACID-BASE EQUILIBRIUM of the body.
UMLS ID:: C0001118
MeSH ID:: D000137

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.076

Synonym(s)

Acid-Base Imbalance

Abnormality of acid-base homeostasis

Acid Base Imbalance

Acid-base imbalances

acid base imbalance

acid base imbalances

acid-base imbalance

acid-base imbalances

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Aspirin	6054600	CTD
2	Cocaine	10452435	CTD
3	Nalidixic Acid	847456	CTD
4	Sodium Bicarbonate	10452435	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Calcium Metabolism Disorders	42.9%
2	Iron Metabolism Disorders	42.9%
3	Phosphorus Metabolism Disorders	42.9%
4	Water-Electrolyte Imbalance	42.9%
5	Lipid Metabolism Disorders	42.9%
6	Mitochondrial Diseases	42.9%
7	Glucose Metabolism Disorders	42.9%
8	Hypercalcemia	40.9%
9	Hypocalcemia	40.9%
10	Milk-Alkali Syndrome	40.9%
11	Wasting Syndrome	38.1%
12	Amyloidosis	31%
13	Calcinosis	31%
14	Hyperglycemia	31%
15	Hyperinsulinism	31%
16	Hyperkalemia	31%
17	Hypernatremia	31%
18	Hypoglycemia	31%
19	Hypokalemia	31%
20	Hyponatremia	31%
21	Xanthomatosis	31%
22	Hypophosphatemia	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	Calciphylaxis	25.4%
34	Hemosiderosis	25.4%
35	Vascular calcification	25.4%
36	Leigh Disease	25.1%
37	Hypolipoproteinemias	24.8%
38	Hyperhomocysteinemia	24.5%
39	Brain Diseases, Metabolic, Inborn	24.2%
40	Carbamoyl-Phosphate Synthase I Deficiency Disease	23.7%
41	Hyperlipidemia, Familial Combined	23.5%
42	Nutrition Disorders	23.1%
43	Hyperlipoproteinemia Type III	22.8%
44	Hypercholesterolemia	22.7%
45	Hyperlipoproteinemias	22.7%
46	Hypertriglyceridemia	22.7%
47	Osteomalacia	22.3%
48	Hypoalphalipoproteinemias	22%
49	Diabetes Mellitus	22%
50	Lactose Intolerance	21.9%
51	Smith-Lemli-Opitz Syndrome	21.1%
52	Galactosemias	21%
53	Urea Cycle Disorders, Inborn	21%
54	Tyrosinemias	21%
55	Dehydration	20.9%
56	Lipomatosis	20.9%
57	Water Intoxication	20.9%
58	Werner Syndrome	20.9%
59	Familial Hypophosphatemic Rickets	20.9%
60	Gaucher Disease	20.6%
61	Congenital Hyperinsulinism	20.5%
62	Amino Acid Metabolism, Inborn Errors	20.5%
63	Bloom Syndrome	20.5%
64	Carbohydrate Metabolism, Inborn Errors	20.5%
65	Metal Metabolism, Inborn Errors	20.5%
66	Osteoporosis	20.5%
67	Progeria	20.5%
68	Lysosomal Storage Diseases	20.5%
69	Bone Demineralization, Pathologic	20.5%
70	Cytochrome-c Oxidase Deficiency	20.5%
71	Peroxisomal Disorders	20.5%
72	Post-Traumatic Osteoporosis	20.5%
73	Celiac Disease	20.2%
74	Sprue, Tropical	20.2%
75	Steatorrhea	20.2%
76	Sprue	20.2%
77	Tay-Sachs Disease	19.4%
78	Glycogen storage disease type II	19.3%
79	Hyperphosphaturia	18.3%
80	Mitochondrial Encephalomyopathies	18.2%
81	Niemann-Pick Disease, Type C	18%
82	Nesidioblastosis	17.9%
83	Homocystinuria	17.9%
84	Amyloid Neuropathies, Familial	17.2%
85	Adiposis Dolorosa	16.9%
86	Alkaptonuria	16.7%
87	Glycogen Storage Disease	16.7%
88	Hypophosphatasia	16.7%
89	Insulin Resistance	16.7%
90	Osteoporosis, Postmenopausal	16.7%
91	Propionic acidemia	16.7%
92	Dihydropyrimidine Dehydrogenase Deficiency	16.7%
93	Cystinosis	16.7%
94	Fabry Disease	15.9%
95	Neuronal Ceroid-Lipofuscinoses	15.7%
96	Mitochondrial Myopathies	15.5%
97	Myelinolysis, Central Pontine	15.4%
98	Glycosuria	15.1%
99	Reye Syndrome	15.1%
100	Hepatic Encephalopathy	15%
101	Glycogen Storage Disease Type I	14.8%
102	Glycogen Storage Disease Type V	14.8%
103	Mucopolysaccharidosis III	14.6%
104	Child Nutrition Disorders	14.3%
105	Hypervitaminosis A	14.3%
106	Infant Nutrition Disorders	14.3%
107	Malnutrition	14.3%
108	MELAS Syndrome	14.1%
109	HIV-Associated Lipodystrophy Syndrome	14.1%
110	Renal Osteodystrophy	13.9%
111	Renal rickets	13.9%
112	Adrenoleukodystrophy	13.7%
113	Zellweger Syndrome	13.5%
114	Menkes Kinky Hair Syndrome	13.3%
115	HIV Wasting Syndrome	13.3%
116	Gestational Diabetes	13%
117	Latent Autoimmune Diabetes in Adults	13%
118	Diabetes Mellitus, Experimental	12.8%
119	Nephrocalcinosis	12.5%
120	Tetany	12.5%
121	Diabetic Ketoacidosis	12.4%
122	Hepatolenticular Degeneration	12.4%
123	Porphyrias, Hepatic	12.3%
124	Cerebral Amyloid Angiopathy	12.3%
125	Wernicke Encephalopathy	12.2%
126	Glycosuria, Renal	12.2%
127	Refsum Disease	12.2%
128	Necrobiosis Lipoidica Diabeticorum	12.1%
129	Fanconi Anemia	11.9%
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	Renal tubular acidosis	8.2%
162	Ataxia Telangiectasia	7.6%
163	Ascorbic Acid Deficiency	7.6%
164	Vitamin A Deficiency	7.6%
165	Vitamin D Deficiency	7.6%
166	Vitamin E Deficiency	7.6%
167	Marasmus	7.6%
168	Optic Atrophy, Hereditary, Leber	7.4%
169	Arthritis, Gouty	7.4%
170	Folic Acid Deficiency	7.1%
171	Pellagra	7.1%
172	Thiamine Deficiency	7.1%
173	Vitamin B 12 Deficiency	7.1%
174	Vitamin B 6 Deficiency	7.1%
175	Pyridoxine Deficiency	7.1%
176	CREST Syndrome	7%
177	Beriberi	6.9%
178	Xeroderma Pigmentosum	6.8%
179	Albinism	6.3%
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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