MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Avitaminosis

(UMLS:C0376286)

Definition:: A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed)
UMLS ID:: C0376286
MeSH ID:: D001361

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654.521.500.133

Synonym(s)

Avitaminosis

AVITAMINOSIS

Avitaminosis, NOS

avitaminoses

avitaminosis

hypovitaminosis

lack of vitamins

vitamin deficiencies

vitamin deficiency

10.

vitamin deficiency syndrome

Associated Drug(s)

	Name	Data Source
1	Acamprosate	SIDER
2	Lansoprazole	SIDER
3	Orlistat	SIDER
4	Pregabalin	SIDER
5	Ritonavir	SIDER
6	Selegiline	SIDER
7	Thalidomide	SIDER

Similar ADE(s)

	Name	Semantic Similarity
1	Magnesium Deficiency	48.4%
2	Potassium Deficiency	48.4%
3	Protein Deficiency	48.4%
4	Marasmus	36%
5	Starvation	34.4%
6	Refeeding Syndrome	34.4%
7	Child Nutrition Disorders	25.4%
8	Hypervitaminosis A	25.4%
9	Infant Nutrition Disorders	25.4%
10	Wasting Syndrome	23%
11	Kwashiorkor	22.6%
12	Metabolic Diseases	16.4%
13	Acid-Base Imbalance	8.5%
14	Calcium Metabolism Disorders	8.5%
15	Iron Metabolism Disorders	8.5%
16	Phosphorus Metabolism Disorders	8.5%
17	Water-Electrolyte Imbalance	8.5%
18	Lipid Metabolism Disorders	8.5%
19	Mitochondrial Diseases	8.5%
20	Glucose Metabolism Disorders	8.5%
21	Hypercalcemia	6.6%
22	Hypocalcemia	6.6%
23	Milk-Alkali Syndrome	6.6%
24	HIV Wasting Syndrome	6.5%
25	Obesity	5.8%
26	Osteopenia	5.7%
27	Brain Diseases, Metabolic	5.6%
28	Lipodystrophy	5%
29	Acidosis	4.9%
30	Alkalosis	4.9%
31	Amyloidosis	4.9%
32	Calcinosis	4.9%
33	Hyperglycemia	4.9%
34	Hyperinsulinism	4.9%
35	Hyperkalemia	4.9%
36	Hypernatremia	4.9%
37	Hypoglycemia	4.9%
38	Hypokalemia	4.9%
39	Hyponatremia	4.9%
40	Xanthomatosis	4.9%
41	Hypophosphatemia	4.9%
42	Metabolic acidosis	4.9%
43	Dyslipidemias	4.9%
44	Iron Overload	4.9%
45	Xanthoma	4.9%
46	Obesity, Abdominal	4.8%
47	Pseudohypoparathyroidism	4.4%
48	Brain Diseases, Metabolic, Inborn	3.9%
49	Rickets	3.9%
50	Pediatric Obesity	3.8%
51	Diabetes Mellitus	3.5%
52	Leigh Disease	3.4%
53	Dehydration	3.4%
54	Lipomatosis	3.4%
55	Water Intoxication	3.4%
56	Werner Syndrome	3.4%
57	Achlorhydria	3.3%
58	Amino Acid Metabolism, Inborn Errors	3.3%
59	Bloom Syndrome	3.3%
60	Carbohydrate Metabolism, Inborn Errors	3.3%
61	Metal Metabolism, Inborn Errors	3.3%
62	Osteoporosis	3.3%
63	Progeria	3.3%
64	Lysosomal Storage Diseases	3.3%
65	Bone Demineralization, Pathologic	3.3%
66	Cytochrome-c Oxidase Deficiency	3.3%
67	Peroxisomal Disorders	3.3%
68	Post-Traumatic Osteoporosis	3.3%
69	Prader-Willi Syndrome	3.3%
70	Celiac Disease	3.3%
71	Sprue, Tropical	3.3%
72	Steatorrhea	3.3%
73	Sprue	3.3%
74	Lactose Intolerance	3.2%
75	Hyperhomocysteinemia	3.2%
76	Acidosis, Lactic	3.2%
77	Calciphylaxis	3.2%
78	Hemosiderosis	3.2%
79	Hypolipoproteinemias	3.2%
80	Ketosis	3.2%
81	Ketonuria	3.2%
82	Ketoacidosis	3.2%
83	Ketonemia	3.2%
84	Vascular calcification	3.2%
85	Carbamoyl-Phosphate Synthase I Deficiency Disease	3%
86	Hyperlipoproteinemia Type IV	2.9%
87	Hyperlipoproteinemia Type V	2.9%
88	Diabetic Ketoacidosis	2.8%
89	Hyperlipidemia, Familial Combined	2.8%
90	Smith-Lemli-Opitz Syndrome	2.8%
91	Galactosemias	2.8%
92	Urea Cycle Disorders, Inborn	2.8%
93	Tyrosinemias	2.8%
94	Mitochondrial Encephalomyopathies	2.7%
95	Congenital Hyperinsulinism	2.7%
96	Hyperlipoproteinemia Type III	2.6%
97	Osteomalacia	2.6%
98	Mitochondrial Myopathies	2.5%
99	Myelinolysis, Central Pontine	2.5%
100	Glycosuria	2.5%
101	Reye Syndrome	2.5%
102	Hepatic Encephalopathy	2.4%
103	Hyperphosphaturia	2.4%
104	Hypercholesterolemia	2.4%
105	Hyperlipoproteinemias	2.4%
106	Hypertriglyceridemia	2.4%
107	Hypoalphalipoproteinemias	2.4%
108	Homocystinuria	2.2%
109	Familial Hypophosphatemic Rickets	2.2%
110	Acidosis, Respiratory	2.2%
111	Adiposis Dolorosa	2.2%
112	Alkalosis, Respiratory	2.2%
113	Alkaptonuria	2.2%
114	Glycogen Storage Disease	2.2%
115	Hypophosphatasia	2.2%
116	Insulin Resistance	2.2%
117	Osteoporosis, Postmenopausal	2.2%
118	Propionic acidemia	2.2%
119	Dihydropyrimidine Dehydrogenase Deficiency	2.2%
120	Cystinosis	2.2%
121	Renal tubular acidosis	2.1%
122	Glycogen storage disease type II	2.1%
123	Gaucher Disease	2.1%
124	Amyloid Neuropathies, Familial	2%
125	Porphyrias, Hepatic	2%
126	Necrobiosis Lipoidica Diabeticorum	2%
127	Fanconi Anemia	1.9%
128	Nesidioblastosis	1.9%
129	Neuronal Ceroid-Lipofuscinoses	1.9%
130	HIV-Associated Lipodystrophy Syndrome	1.8%
131	Zellweger Syndrome	1.8%
132	MELAS Syndrome	1.8%
133	Menkes Kinky Hair Syndrome	1.8%
134	Adrenoleukodystrophy	1.7%
135	Gestational Diabetes	1.7%
136	Latent Autoimmune Diabetes in Adults	1.7%
137	Tay-Sachs Disease	1.7%
138	Diabetes Mellitus, Experimental	1.7%
139	Niemann-Pick Disease, Type C	1.6%
140	Hepatolenticular Degeneration	1.6%
141	Wernicke Encephalopathy	1.6%
142	Nephrocalcinosis	1.6%
143	Tetany	1.6%
144	Friedreich Ataxia	1.6%
145	Renal Osteodystrophy	1.6%
146	Renal rickets	1.6%
147	Refsum Disease	1.6%
148	Glycosuria, Renal	1.6%
149	Cerebral Amyloid Angiopathy	1.6%
150	Glycogen Storage Disease Type I	1.6%
151	Glycogen Storage Disease Type V	1.6%
152	Mucopolysaccharidosis III	1.6%
153	Fabry Disease	1.6%
154	Kernicterus	1.4%
155	Cockayne Syndrome	1.4%
156	Familial Periodic Paralysis	1.3%
157	Primary amyloidosis	1.3%
158	Kearns-Sayre syndrome	1.3%
159	Variegate Porphyria	1.3%
160	Acute intermittent porphyria	1.3%
161	Porphyria Cutanea Tarda	1.3%
162	Renal Aminoacidurias	1.3%
163	Fanconi Syndrome	1.3%
164	Pseudohypoaldosteronism	1.3%
165	Liddle Syndrome	1.3%
166	Ataxia Telangiectasia	1.3%
167	Optic Atrophy, Hereditary, Leber	1.2%
168	Sjogren-Larsson Syndrome	1.1%
169	Xeroderma Pigmentosum	1.1%
170	Gout	1.1%
171	Amyotrophic Lateral Sclerosis	1.1%
172	Antley-Bixler Syndrome Phenotype	1.1%
173	Canavan Disease	1.1%
174	Alexander Disease	1.1%
175	Mucopolysaccharidosis II	1.1%
176	Hypokalemic periodic paralysis	1%
177	Frontotemporal dementia	1%
178	Cystinuria	1%
179	CREST Syndrome	0.9%
180	Albinism	0.8%
181	Arthritis, Gouty	0.8%
182	Ichthyosis, X-Linked	0.7%

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