MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Milk-Alkali Syndrome

(UMLS:C0026141)

UMLS ID:: C0026141
MeSH ID:: D006934

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.174.451|C18.452.950.340

Synonym(s)

Milk-Alkali Syndrome

BURNETT SYNDROME

Burnett

Burnett's syndrome

MILK DRINKER SYNDROME

MILK-ALKALI SYNDROME

Milk alkali syndrome

Milk-alkali syndrome

burnett syndrome

10.

burnett's syndrome

11.

drinkers milk syndrome

12.

milk alkali syndrome

13.

milk-alkali syndrome

14.

milk-alkali; syndrome

15.

syndrome; milk-alkali

Associated Drug(s)

	Name	Number of Reports	Data Source
1	Calcium Carbonate	FAERS: 26 Canada Vigilance: 2	Canada Vigilance US FAERS
2	Hydrochlorothiazide	FAERS: 2	US FAERS
3	Magnesium Oxide	FAERS: 1	US FAERS
4	Metolazone		OFFSIDES

Similar ADE(s)

	Name	Semantic Similarity
1	Hypocalcemia	66.7%
2	Calcinosis	44.4%
3	Hyperkalemia	44.4%
4	Hypernatremia	44.4%
5	Hypokalemia	44.4%
6	Hyponatremia	44.4%
7	Wasting Syndrome	41.4%
8	Acid-Base Imbalance	40.9%
9	Iron Metabolism Disorders	40.9%
10	Phosphorus Metabolism Disorders	40.9%
11	Lipid Metabolism Disorders	40.9%
12	Mitochondrial Diseases	40.9%
13	Glucose Metabolism Disorders	40.9%
14	Pseudohypoparathyroidism	38.7%
15	Rickets	37.7%
16	Dehydration	33.9%
17	Water Intoxication	33.9%
18	Calciphylaxis	33%
19	Vascular calcification	33%
20	Lipodystrophy	32%
21	Osteopenia	31%
22	Brain Diseases, Metabolic	30.5%
23	Osteomalacia	28.3%
24	Leigh Disease	27%
25	Acidosis	26.7%
26	Alkalosis	26.7%
27	Amyloidosis	26.7%
28	Hyperglycemia	26.7%
29	Hyperinsulinism	26.7%
30	Hypoglycemia	26.7%
31	Xanthomatosis	26.7%
32	Hypophosphatemia	26.7%
33	Metabolic acidosis	26.7%
34	Dyslipidemias	26.7%
35	Iron Overload	26.7%
36	Xanthoma	26.7%
37	Brain Diseases, Metabolic, Inborn	26.5%
38	Hyperhomocysteinemia	25.3%
39	Carbamoyl-Phosphate Synthase I Deficiency Disease	24.7%
40	Hyperlipoproteinemia Type IV	24.3%
41	Hyperlipoproteinemia Type V	24.3%
42	Nutrition Disorders	23.8%
43	Familial Hypophosphatemic Rickets	23.7%
44	Hypolipoproteinemias	23.5%
45	Lactose Intolerance	23%
46	Smith-Lemli-Opitz Syndrome	22%
47	Galactosemias	21.9%
48	Urea Cycle Disorders, Inborn	21.9%
49	Tyrosinemias	21.9%
50	Diabetic Ketoacidosis	21.6%
51	Hyperlipidemia, Familial Combined	21.5%
52	Diabetes Mellitus	21.1%
53	Hyperlipoproteinemia Type III	20.5%
54	Calcium Metabolism Disorders	20.5%
55	Water-Electrolyte Imbalance	20.5%
56	Lipomatosis	20.3%
57	Werner Syndrome	20.3%
58	Congenital Hyperinsulinism	20.2%
59	Achlorhydria	20%
60	Amino Acid Metabolism, Inborn Errors	20%
61	Bloom Syndrome	20%
62	Carbohydrate Metabolism, Inborn Errors	20%
63	Hypercalcemia	20%
64	Metal Metabolism, Inborn Errors	20%
65	Milk-Alkali Syndrome	20%
66	Osteoporosis	20%
67	Progeria	20%
68	Lysosomal Storage Diseases	20%
69	Bone Demineralization, Pathologic	20%
70	Cytochrome-c Oxidase Deficiency	20%
71	Peroxisomal Disorders	20%
72	Post-Traumatic Osteoporosis	20%
73	Gaucher Disease	20%
74	Celiac Disease	19.8%
75	Sprue, Tropical	19.8%
76	Steatorrhea	19.8%
77	Sprue	19.8%
78	Acidosis, Lactic	19.8%
79	Hemosiderosis	19.8%
80	Ketosis	19.8%
81	Ketonuria	19.8%
82	Ketoacidosis	19.8%
83	Ketonemia	19.8%
84	Nephrocalcinosis	19.7%
85	Tetany	19.7%
86	Mitochondrial Encephalomyopathies	19.7%
87	Hyperphosphaturia	19.5%
88	Hypoalphalipoproteinemias	19.4%
89	Glycogen storage disease type II	19.2%
90	Renal Osteodystrophy	18.9%
91	Renal rickets	18.9%
92	Homocystinuria	18.5%
93	Tay-Sachs Disease	17.9%
94	Amyloid Neuropathies, Familial	17.4%
95	Niemann-Pick Disease, Type C	17%
96	Renal tubular acidosis	16.7%
97	Hypercholesterolemia	16.4%
98	Hyperlipoproteinemias	16.4%
99	Hypertriglyceridemia	16.4%
100	Nesidioblastosis	16.4%
101	Mitochondrial Myopathies	16.2%
102	Myelinolysis, Central Pontine	16.1%
103	Glycosuria	15.9%
104	Reye Syndrome	15.9%
105	Hepatic Encephalopathy	15.8%
106	Fabry Disease	15.7%
107	Neuronal Ceroid-Lipofuscinoses	15.4%
108	Adrenoleukodystrophy	15.1%
109	HIV Wasting Syndrome	15.1%
110	MELAS Syndrome	15%
111	Acidosis, Respiratory	14.9%
112	Adiposis Dolorosa	14.9%
113	Alkalosis, Respiratory	14.9%
114	Zellweger Syndrome	14.8%
115	Alkaptonuria	14.8%
116	Glycogen Storage Disease	14.8%
117	Hypophosphatasia	14.8%
118	Insulin Resistance	14.8%
119	Osteoporosis, Postmenopausal	14.8%
120	Propionic acidemia	14.8%
121	Dihydropyrimidine Dehydrogenase Deficiency	14.8%
122	Cystinosis	14.8%
123	HIV-Associated Lipodystrophy Syndrome	14.7%
124	Menkes Kinky Hair Syndrome	14.6%
125	Mucopolysaccharidosis III	13.8%
126	Hepatolenticular Degeneration	13.7%
127	Child Nutrition Disorders	13.6%
128	Hypervitaminosis A	13.6%
129	Infant Nutrition Disorders	13.6%
130	Malnutrition	13.6%
131	Porphyrias, Hepatic	13.5%
132	Refsum Disease	13.5%
133	Wernicke Encephalopathy	13.3%
134	Necrobiosis Lipoidica Diabeticorum	13.3%
135	Fanconi Anemia	13.1%
136	Glycosuria, Renal	12.9%
137	Gestational Diabetes	12.2%
138	Latent Autoimmune Diabetes in Adults	12.2%
139	CREST Syndrome	12.2%
140	Glycogen Storage Disease Type I	12.2%
141	Glycogen Storage Disease Type V	12.2%
142	Diabetes Mellitus, Experimental	12.1%
143	Cerebral Amyloid Angiopathy	11.7%
144	Friedreich Ataxia	11.2%
145	Kearns-Sayre syndrome	10.5%
146	Kernicterus	10%
147	Familial Periodic Paralysis	10%
148	Cockayne Syndrome	10%
149	Primary amyloidosis	9.9%
150	Variegate Porphyria	9.8%
151	Acute intermittent porphyria	9.8%
152	Porphyria Cutanea Tarda	9.8%
153	Sjogren-Larsson Syndrome	9.8%
154	Renal Aminoacidurias	9.8%
155	Fanconi Syndrome	9.8%
156	Pseudohypoaldosteronism	9.8%
157	Liddle Syndrome	9.8%
158	Canavan Disease	9.7%
159	Alexander Disease	9.7%
160	Mucopolysaccharidosis II	9.7%
161	Ataxia Telangiectasia	9%
162	Deficiency Diseases	8.9%
163	Starvation	8.9%
164	Refeeding Syndrome	8.9%
165	Optic Atrophy, Hereditary, Leber	8.7%
166	Gout	8.6%
167	Amyotrophic Lateral Sclerosis	8.5%
168	Antley-Bixler Syndrome Phenotype	8.4%
169	Hypokalemic periodic paralysis	8.2%
170	Frontotemporal dementia	8.1%
171	Cystinuria	8.1%
172	Xeroderma Pigmentosum	8.1%
173	Arthritis, Gouty	7%
174	Albinism	6.6%
175	Kwashiorkor	6.6%
176	Magnesium Deficiency	6.6%
177	Potassium Deficiency	6.6%
178	Protein Deficiency	6.6%
179	Avitaminosis	6.6%
180	Ascorbic Acid Deficiency	5.5%
181	Vitamin A Deficiency	5.5%
182	Vitamin D Deficiency	5.5%
183	Vitamin E Deficiency	5.5%
184	Marasmus	5.5%
185	Ichthyosis, X-Linked	5.4%
186	Folic Acid Deficiency	4.9%
187	Pellagra	4.9%
188	Thiamine Deficiency	4.9%
189	Vitamin B 12 Deficiency	4.9%
190	Vitamin B 6 Deficiency	4.9%
191	Pyridoxine Deficiency	4.9%
192	Beriberi	4.6%
193	Obesity	4.3%
194	Obesity, Abdominal	3.9%
195	Anemia, Pernicious	3.4%
196	Vitamin K Deficiency	3.3%
197	Pediatric Obesity	3.2%
198	Scurvy	2.9%
199	Prader-Willi Syndrome	2.8%
200	Subacute Combined Degeneration	2%

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