MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Pyridoxine Deficiency

(UMLS:C1527330)

Definition:: Deficiency of PYRIDOXINE, one of the VITAMIN B 6 compounds. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
UMLS ID:: C1527330
MeSH ID:: D026681

Classification:

Name:

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

Synonym(s)

Pyridoxine Deficiency

Pyridoxal deficiency

Pyridoxamine deficiency

Pyridoxine deficiency

deficiency; pyridoxamine

deficiency; pyridoxine

pyridoxamine; deficiency

pyridoxine (vitamin B6) deficiency

pyridoxine deficiency

10.

pyridoxine; deficiency

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Isoniazid			SIDER
2	Penicillamine			SIDER

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%

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