MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Beriberi

(UMLS:C0005122)

Definition:: A disease caused by a deficiency of thiamine (vitamin B1) and characterized by polyneuritis, cardiac pathology, and edema. The epidemic form is found primarily in areas in which white (polished) rice is the staple food, as in Japan, China, the Philippines, India, and other countries of southeast Asia. (Dorland, 27th ed)
UMLS ID:: C0005122
MeSH ID:: D001602

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654.521.500.133.699.827.223

Synonym(s)

Beriberi

Beri Beri

Beri-beri

Beriberi, NOS

Kakk猫

POLYNEURITIS, ENDEMIC

Thiamine Deficiency

Vitamin B1 Deficiency

beri beri

10.

beri-beri

11.

beriberi

12.

bery bery

13.

deficiency; vitamin, B1, beriberi

14.

deficiency; vitamin, thiamine, beriberi

15.

endemic polyneuritis

16.

vitamin; deficiency, B1, beriberi

17.

vitamin; deficiency, thiamine, beriberi

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Thiamine		31419397	CTD
2	citreoviridin		31419397	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Folic Acid Deficiency	37.1%
2	Pellagra	37.1%
3	Vitamin B 12 Deficiency	37.1%
4	Vitamin B 6 Deficiency	37.1%
5	Pyridoxine Deficiency	37.1%
6	Ascorbic Acid Deficiency	30.6%
7	Vitamin A Deficiency	30.6%
8	Vitamin D Deficiency	30.6%
9	Vitamin E Deficiency	30.6%
10	Magnesium Deficiency	26.8%
11	Potassium Deficiency	26.8%
12	Protein Deficiency	26.8%
13	Starvation	24%
14	Refeeding Syndrome	24%
15	Child Nutrition Disorders	20.7%
16	Hypervitaminosis A	20.7%
17	Infant Nutrition Disorders	20.7%
18	Wasting Syndrome	18.8%
19	Wernicke Encephalopathy	18.3%
20	Hyperhomocysteinemia	17.3%
21	Anemia, Pernicious	16.5%
22	Vitamin K Deficiency	15.7%
23	Marasmus	14.8%
24	Metabolic Diseases	14.5%
25	Kwashiorkor	12.5%
26	Rickets	10.3%
27	Scurvy	9.3%
28	Subacute Combined Degeneration	8.8%
29	Acid-Base Imbalance	6.9%
30	Calcium Metabolism Disorders	6.9%
31	Iron Metabolism Disorders	6.9%
32	Phosphorus Metabolism Disorders	6.9%
33	Water-Electrolyte Imbalance	6.9%
34	Lipid Metabolism Disorders	6.9%
35	Mitochondrial Diseases	6.9%
36	Glucose Metabolism Disorders	6.9%
37	Osteomalacia	6.4%
38	Osteopenia	4.7%
39	Hypercalcemia	4.6%
40	Hypocalcemia	4.6%
41	Milk-Alkali Syndrome	4.6%
42	HIV Wasting Syndrome	4.6%
43	Brain Diseases, Metabolic	4.6%
44	Obesity	4.1%
45	Renal Osteodystrophy	4%
46	Renal rickets	4%
47	Lipodystrophy	3.5%
48	Acidosis	3.4%
49	Alkalosis	3.4%
50	Amyloidosis	3.4%
51	Calcinosis	3.4%
52	Hyperglycemia	3.4%
53	Hyperinsulinism	3.4%
54	Hyperkalemia	3.4%
55	Hypernatremia	3.4%
56	Hypoglycemia	3.4%
57	Hypokalemia	3.4%
58	Hyponatremia	3.4%
59	Xanthomatosis	3.4%
60	Hypophosphatemia	3.4%
61	Metabolic acidosis	3.4%
62	Dyslipidemias	3.4%
63	Iron Overload	3.4%
64	Xanthoma	3.4%
65	Pseudohypoparathyroidism	2.9%
66	Brain Diseases, Metabolic, Inborn	2.8%
67	Obesity, Abdominal	2.7%
68	Diabetes Mellitus	2.5%
69	Dehydration	2.4%
70	Lipomatosis	2.4%
71	Water Intoxication	2.4%
72	Werner Syndrome	2.4%
73	Familial Hypophosphatemic Rickets	2.3%
74	Achlorhydria	2.3%
75	Amino Acid Metabolism, Inborn Errors	2.3%
76	Bloom Syndrome	2.3%
77	Carbohydrate Metabolism, Inborn Errors	2.3%
78	Metal Metabolism, Inborn Errors	2.3%
79	Osteoporosis	2.3%
80	Progeria	2.3%
81	Lysosomal Storage Diseases	2.3%
82	Bone Demineralization, Pathologic	2.3%
83	Cytochrome-c Oxidase Deficiency	2.3%
84	Peroxisomal Disorders	2.3%
85	Post-Traumatic Osteoporosis	2.3%
86	Celiac Disease	2.3%
87	Sprue, Tropical	2.3%
88	Steatorrhea	2.3%
89	Sprue	2.3%
90	Pediatric Obesity	2.1%
91	Lactose Intolerance	2.1%
92	Leigh Disease	2%
93	Prader-Willi Syndrome	1.8%
94	Hypolipoproteinemias	1.8%
95	Acidosis, Lactic	1.8%
96	Calciphylaxis	1.8%
97	Hemosiderosis	1.8%
98	Ketosis	1.8%
99	Ketonuria	1.8%
100	Ketoacidosis	1.8%
101	Ketonemia	1.8%
102	Vascular calcification	1.8%
103	Mitochondrial Myopathies	1.8%
104	Myelinolysis, Central Pontine	1.8%
105	Mitochondrial Encephalomyopathies	1.8%
106	Glycosuria	1.7%
107	Reye Syndrome	1.7%
108	Hepatic Encephalopathy	1.7%
109	Carbamoyl-Phosphate Synthase I Deficiency Disease	1.6%
110	Smith-Lemli-Opitz Syndrome	1.6%
111	Galactosemias	1.5%
112	Urea Cycle Disorders, Inborn	1.5%
113	Tyrosinemias	1.5%
114	Congenital Hyperinsulinism	1.5%
115	Porphyrias, Hepatic	1.4%
116	Diabetic Ketoacidosis	1.4%
117	Hyperlipidemia, Familial Combined	1.4%
118	Necrobiosis Lipoidica Diabeticorum	1.4%
119	Fanconi Anemia	1.4%
120	Hyperphosphaturia	1.4%
121	Acidosis, Respiratory	1.2%
122	Adiposis Dolorosa	1.2%
123	Alkalosis, Respiratory	1.2%
124	Renal tubular acidosis	1.2%
125	Alkaptonuria	1.2%
126	Glycogen Storage Disease	1.2%
127	Hypophosphatasia	1.2%
128	Insulin Resistance	1.2%
129	Osteoporosis, Postmenopausal	1.2%
130	Propionic acidemia	1.2%
131	Dihydropyrimidine Dehydrogenase Deficiency	1.2%
132	Cystinosis	1.2%
133	Hyperlipoproteinemia Type III	1.2%
134	Hyperlipoproteinemia Type IV	1.2%
135	Hyperlipoproteinemia Type V	1.2%
136	Homocystinuria	1.2%
137	Friedreich Ataxia	1.1%
138	HIV-Associated Lipodystrophy Syndrome	1%
139	Kernicterus	1%
140	Zellweger Syndrome	1%
141	Cockayne Syndrome	1%
142	Hypoalphalipoproteinemias	1%
143	Menkes Kinky Hair Syndrome	1%
144	Hypercholesterolemia	1%
145	Hyperlipoproteinemias	1%
146	Hypertriglyceridemia	1%
147	Amyloid Neuropathies, Familial	1%
148	Gestational Diabetes	0.9%
149	Latent Autoimmune Diabetes in Adults	0.9%
150	Neuronal Ceroid-Lipofuscinoses	0.9%
151	Diabetes Mellitus, Experimental	0.9%
152	MELAS Syndrome	0.9%
153	Hepatolenticular Degeneration	0.9%
154	Nephrocalcinosis	0.9%
155	Tetany	0.9%
156	Refsum Disease	0.9%
157	Glycosuria, Renal	0.9%
158	Cerebral Amyloid Angiopathy	0.9%
159	Ataxia Telangiectasia	0.9%
160	Glycogen storage disease type II	0.9%
161	Adrenoleukodystrophy	0.9%
162	Optic Atrophy, Hereditary, Leber	0.9%
163	Nesidioblastosis	0.8%
164	Kearns-Sayre syndrome	0.8%
165	Xeroderma Pigmentosum	0.8%
166	Familial Periodic Paralysis	0.7%
167	Primary amyloidosis	0.7%
168	Variegate Porphyria	0.7%
169	Acute intermittent porphyria	0.7%
170	Porphyria Cutanea Tarda	0.7%
171	Renal Aminoacidurias	0.7%
172	Fanconi Syndrome	0.7%
173	Pseudohypoaldosteronism	0.7%
174	Liddle Syndrome	0.7%
175	Gaucher Disease	0.7%
176	Mucopolysaccharidosis III	0.7%
177	Glycogen Storage Disease Type I	0.7%
178	Glycogen Storage Disease Type V	0.7%
179	Gout	0.6%
180	Amyotrophic Lateral Sclerosis	0.6%
181	Antley-Bixler Syndrome Phenotype	0.6%
182	Sjogren-Larsson Syndrome	0.6%
183	Fabry Disease	0.5%
184	CREST Syndrome	0.5%
185	Albinism	0.5%
186	Canavan Disease	0.4%
187	Alexander Disease	0.4%
188	Mucopolysaccharidosis II	0.4%
189	Hypokalemic periodic paralysis	0.4%
190	Frontotemporal dementia	0.4%
191	Cystinuria	0.4%
192	Niemann-Pick Disease, Type C	0.4%
193	Ichthyosis, X-Linked	0.4%
194	Arthritis, Gouty	0.3%
195	Tay-Sachs Disease	0.3%

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