MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Vitamin B 6 Deficiency

(UMLS:C0936215)

Definition:: A nutritional condition produced by a deficiency of VITAMIN B 6 in the diet, characterized by dermatitis, glossitis, cheilosis, and stomatitis. Marked deficiency causes irritability, weakness, depression, dizziness, peripheral neuropathy, and seizures. In infants and children typical manifestations are diarrhea, anemia, and seizures. Deficiency can be caused by certain medications, such as isoniazid.
UMLS ID:: C0936215
MeSH ID:: D026681

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654.521.500.133.699.901

Synonym(s)

Vitamin B 6 Deficiency

Pyridoxine Deficiency

Pyridoxine Deficincy

Reduced circulating vitamin B6 level

Reduced vitamin b6 levels

VITAMIN B6 DEFICIENCY

VITAMIN DEFICIENCY B6

Vitamin B6 Deficiency

Vitamin B6 deficiency

10.

Vitamin B6 deficiency disease

11.

b6 deficiency diseases vitamin

12.

b6 deficiency vitamin

13.

deficiency; vitamin, B6

14.

syndrome; vitamin B6 deficiency

15.

vitamin B6 deficiency

16.

vitamin B6; deficiency syndrome

17.

vitamin b6 deficiency

18.

vitamin; deficiency, B6

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Isoniazid	4353461	CTD
2	Penicillamine	3341945 5421930	CTD
3	Pyridoxal Phosphate	3341945	CTD
4	Ribavirin	19042060	CTD
5	Vitamin B 6	3341945	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Folic Acid Deficiency	49.6%
2	Pellagra	49.6%
3	Thiamine Deficiency	49.6%
4	Vitamin B 12 Deficiency	49.6%
5	Beriberi	37.1%
6	Ascorbic Acid Deficiency	36.8%
7	Vitamin A Deficiency	36.8%
8	Vitamin D Deficiency	36.8%
9	Vitamin E Deficiency	36.8%
10	Magnesium Deficiency	29.9%
11	Potassium Deficiency	29.9%
12	Protein Deficiency	29.9%
13	Starvation	25.5%
14	Refeeding Syndrome	25.5%
15	Anemia, Pernicious	24.8%
16	Hyperhomocysteinemia	22.5%
17	Child Nutrition Disorders	21.3%
18	Hypervitaminosis A	21.3%
19	Infant Nutrition Disorders	21.3%
20	Wasting Syndrome	19.4%
21	Vitamin K Deficiency	18.9%
22	Marasmus	17.8%
23	Metabolic Diseases	14.8%
24	Wernicke Encephalopathy	14%
25	Kwashiorkor	13.9%
26	Subacute Combined Degeneration	13.2%
27	Rickets	13%
28	Scurvy	12.4%
29	Osteomalacia	9%
30	Acid-Base Imbalance	7.1%
31	Calcium Metabolism Disorders	7.1%
32	Iron Metabolism Disorders	7.1%
33	Phosphorus Metabolism Disorders	7.1%
34	Water-Electrolyte Imbalance	7.1%
35	Lipid Metabolism Disorders	7.1%
36	Mitochondrial Diseases	7.1%
37	Glucose Metabolism Disorders	7.1%
38	Renal Osteodystrophy	5.7%
39	Renal rickets	5.7%
40	Hypercalcemia	4.9%
41	Hypocalcemia	4.9%
42	Milk-Alkali Syndrome	4.9%
43	HIV Wasting Syndrome	4.9%
44	Osteopenia	4.8%
45	Brain Diseases, Metabolic	4.7%
46	Obesity	4.3%
47	Lipodystrophy	3.7%
48	Acidosis	3.6%
49	Alkalosis	3.6%
50	Amyloidosis	3.6%
51	Calcinosis	3.6%
52	Hyperglycemia	3.6%
53	Hyperinsulinism	3.6%
54	Hyperkalemia	3.6%
55	Hypernatremia	3.6%
56	Hypoglycemia	3.6%
57	Hypokalemia	3.6%
58	Hyponatremia	3.6%
59	Xanthomatosis	3.6%
60	Hypophosphatemia	3.6%
61	Metabolic acidosis	3.6%
62	Dyslipidemias	3.6%
63	Iron Overload	3.6%
64	Xanthoma	3.6%
65	Familial Hypophosphatemic Rickets	3.5%
66	Pseudohypoparathyroidism	3.1%
67	Obesity, Abdominal	3%
68	Brain Diseases, Metabolic, Inborn	2.9%
69	Diabetes Mellitus	2.6%
70	Dehydration	2.5%
71	Lipomatosis	2.5%
72	Water Intoxication	2.5%
73	Werner Syndrome	2.5%
74	Achlorhydria	2.5%
75	Amino Acid Metabolism, Inborn Errors	2.5%
76	Bloom Syndrome	2.5%
77	Carbohydrate Metabolism, Inborn Errors	2.5%
78	Metal Metabolism, Inborn Errors	2.5%
79	Osteoporosis	2.5%
80	Progeria	2.5%
81	Lysosomal Storage Diseases	2.5%
82	Bone Demineralization, Pathologic	2.5%
83	Cytochrome-c Oxidase Deficiency	2.5%
84	Peroxisomal Disorders	2.5%
85	Post-Traumatic Osteoporosis	2.5%
86	Celiac Disease	2.4%
87	Sprue, Tropical	2.4%
88	Steatorrhea	2.4%
89	Sprue	2.4%
90	Pediatric Obesity	2.4%
91	Lactose Intolerance	2.3%
92	Leigh Disease	2.2%
93	Prader-Willi Syndrome	2%
94	Hypolipoproteinemias	2%
95	Acidosis, Lactic	2%
96	Calciphylaxis	2%
97	Hemosiderosis	2%
98	Ketosis	2%
99	Ketonuria	2%
100	Ketoacidosis	2%
101	Ketonemia	2%
102	Vascular calcification	2%
103	Mitochondrial Encephalomyopathies	1.9%
104	Mitochondrial Myopathies	1.9%
105	Myelinolysis, Central Pontine	1.9%
106	Glycosuria	1.8%
107	Reye Syndrome	1.8%
108	Hepatic Encephalopathy	1.8%
109	Carbamoyl-Phosphate Synthase I Deficiency Disease	1.8%
110	Smith-Lemli-Opitz Syndrome	1.7%
111	Galactosemias	1.7%
112	Urea Cycle Disorders, Inborn	1.7%
113	Tyrosinemias	1.7%
114	Congenital Hyperinsulinism	1.7%
115	Diabetic Ketoacidosis	1.6%
116	Hyperlipidemia, Familial Combined	1.6%
117	Hyperphosphaturia	1.5%
118	Porphyrias, Hepatic	1.5%
119	Necrobiosis Lipoidica Diabeticorum	1.5%
120	Fanconi Anemia	1.5%
121	Hyperlipoproteinemia Type IV	1.4%
122	Hyperlipoproteinemia Type V	1.4%
123	Hyperlipoproteinemia Type III	1.4%
124	Acidosis, Respiratory	1.3%
125	Adiposis Dolorosa	1.3%
126	Alkalosis, Respiratory	1.3%
127	Renal tubular acidosis	1.3%
128	Alkaptonuria	1.3%
129	Glycogen Storage Disease	1.3%
130	Hypophosphatasia	1.3%
131	Insulin Resistance	1.3%
132	Osteoporosis, Postmenopausal	1.3%
133	Propionic acidemia	1.3%
134	Dihydropyrimidine Dehydrogenase Deficiency	1.3%
135	Cystinosis	1.3%
136	Homocystinuria	1.3%
137	Friedreich Ataxia	1.2%
138	Hypoalphalipoproteinemias	1.2%
139	Hypercholesterolemia	1.2%
140	Hyperlipoproteinemias	1.2%
141	Hypertriglyceridemia	1.2%
142	HIV-Associated Lipodystrophy Syndrome	1.2%
143	Zellweger Syndrome	1.1%
144	Amyloid Neuropathies, Familial	1.1%
145	Menkes Kinky Hair Syndrome	1.1%
146	Neuronal Ceroid-Lipofuscinoses	1.1%
147	Kernicterus	1.1%
148	Cockayne Syndrome	1.1%
149	Glycogen storage disease type II	1.1%
150	Gestational Diabetes	1.1%
151	Latent Autoimmune Diabetes in Adults	1.1%
152	MELAS Syndrome	1%
153	Diabetes Mellitus, Experimental	1%
154	Hepatolenticular Degeneration	1%
155	Nephrocalcinosis	1%
156	Tetany	1%
157	Refsum Disease	1%
158	Glycosuria, Renal	1%
159	Cerebral Amyloid Angiopathy	1%
160	Adrenoleukodystrophy	1%
161	Nesidioblastosis	1%
162	Ataxia Telangiectasia	0.9%
163	Optic Atrophy, Hereditary, Leber	0.9%
164	Kearns-Sayre syndrome	0.9%
165	Gaucher Disease	0.9%
166	Xeroderma Pigmentosum	0.8%
167	Familial Periodic Paralysis	0.8%
168	Primary amyloidosis	0.8%
169	Variegate Porphyria	0.8%
170	Acute intermittent porphyria	0.8%
171	Porphyria Cutanea Tarda	0.8%
172	Renal Aminoacidurias	0.8%
173	Fanconi Syndrome	0.8%
174	Pseudohypoaldosteronism	0.8%
175	Liddle Syndrome	0.8%
176	Mucopolysaccharidosis III	0.8%
177	Glycogen Storage Disease Type I	0.8%
178	Glycogen Storage Disease Type V	0.8%
179	Gout	0.7%
180	Amyotrophic Lateral Sclerosis	0.7%
181	Antley-Bixler Syndrome Phenotype	0.7%
182	Fabry Disease	0.7%
183	Sjogren-Larsson Syndrome	0.6%
184	CREST Syndrome	0.6%
185	Niemann-Pick Disease, Type C	0.6%
186	Canavan Disease	0.5%
187	Alexander Disease	0.5%
188	Mucopolysaccharidosis II	0.5%
189	Albinism	0.5%
190	Tay-Sachs Disease	0.5%
191	Hypokalemic periodic paralysis	0.5%
192	Frontotemporal dementia	0.5%
193	Cystinuria	0.5%
194	Ichthyosis, X-Linked	0.4%
195	Arthritis, Gouty	0.4%

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