MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Calcium Metabolism Disorders

(UMLS:C0006705)

Definition:: Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization.
UMLS ID:: C0006705
MeSH ID:: D002128

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.174

Synonym(s)

Calcium Metabolism Disorders

CALCIUM METABOLISM DISORDER

Calcium metabolism disorder

Calcium--Metabolism--Disorders

Disorder of calcium metabolism

Disorder of calcium metabolism, NOS

Disorders of calcium metabolism

Unspecified disorder of calcium metabolism

calcium metabolism disorders

10.

calcium; metabolic disorder

11.

disorder of calcium metabolism

12.

metabolic disorder; calcium

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Calcitriol		6688127	CTD
2	Gentamicins		1560382	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Acid-Base Imbalance	42.9%
2	Iron Metabolism Disorders	42.9%
3	Phosphorus Metabolism Disorders	42.9%
4	Water-Electrolyte Imbalance	42.9%
5	Lipid Metabolism Disorders	42.9%
6	Mitochondrial Diseases	42.9%
7	Glucose Metabolism Disorders	42.9%
8	Wasting Syndrome	38.1%
9	Acidosis	31%
10	Alkalosis	31%
11	Amyloidosis	31%
12	Hyperglycemia	31%
13	Hyperinsulinism	31%
14	Hyperkalemia	31%
15	Hypernatremia	31%
16	Hypoglycemia	31%
17	Hypokalemia	31%
18	Hyponatremia	31%
19	Xanthomatosis	31%
20	Hypophosphatemia	31%
21	Metabolic acidosis	31%
22	Dyslipidemias	31%
23	Iron Overload	31%
24	Xanthoma	31%
25	Lipodystrophy	30.5%
26	Osteopenia	28.6%
27	Brain Diseases, Metabolic	27.9%
28	Hyperlipoproteinemia Type IV	26.4%
29	Hyperlipoproteinemia Type V	26.4%
30	Acidosis, Lactic	25.4%
31	Hemosiderosis	25.4%
32	Ketosis	25.4%
33	Ketonuria	25.4%
34	Ketoacidosis	25.4%
35	Ketonemia	25.4%
36	Leigh Disease	25.1%
37	Hypolipoproteinemias	24.8%
38	Hyperhomocysteinemia	24.5%
39	Brain Diseases, Metabolic, Inborn	24.2%
40	Carbamoyl-Phosphate Synthase I Deficiency Disease	23.7%
41	Diabetic Ketoacidosis	23.7%
42	Hyperlipidemia, Familial Combined	23.5%
43	Nutrition Disorders	23.1%
44	Hyperlipoproteinemia Type III	22.8%
45	Hypercholesterolemia	22.7%
46	Hyperlipoproteinemias	22.7%
47	Hypertriglyceridemia	22.7%
48	Hypoalphalipoproteinemias	22%
49	Diabetes Mellitus	22%
50	Lactose Intolerance	21.9%
51	Smith-Lemli-Opitz Syndrome	21.1%
52	Galactosemias	21%
53	Urea Cycle Disorders, Inborn	21%
54	Tyrosinemias	21%
55	Dehydration	20.9%
56	Lipomatosis	20.9%
57	Water Intoxication	20.9%
58	Werner Syndrome	20.9%
59	Gaucher Disease	20.6%
60	Congenital Hyperinsulinism	20.5%
61	Achlorhydria	20.5%
62	Amino Acid Metabolism, Inborn Errors	20.5%
63	Bloom Syndrome	20.5%
64	Carbohydrate Metabolism, Inborn Errors	20.5%
65	Hypercalcemia	20.5%
66	Hypocalcemia	20.5%
67	Metal Metabolism, Inborn Errors	20.5%
68	Milk-Alkali Syndrome	20.5%
69	Osteoporosis	20.5%
70	Progeria	20.5%
71	Lysosomal Storage Diseases	20.5%
72	Bone Demineralization, Pathologic	20.5%
73	Cytochrome-c Oxidase Deficiency	20.5%
74	Peroxisomal Disorders	20.5%
75	Post-Traumatic Osteoporosis	20.5%
76	Celiac Disease	20.2%
77	Sprue, Tropical	20.2%
78	Steatorrhea	20.2%
79	Sprue	20.2%
80	Tay-Sachs Disease	19.4%
81	Glycogen storage disease type II	19.3%
82	Pseudohypoparathyroidism	18.3%
83	Hyperphosphaturia	18.3%
84	Mitochondrial Encephalomyopathies	18.2%
85	Niemann-Pick Disease, Type C	18%
86	Nesidioblastosis	17.9%
87	Homocystinuria	17.9%
88	Familial Hypophosphatemic Rickets	17.6%
89	Amyloid Neuropathies, Familial	17.2%
90	Acidosis, Respiratory	16.9%
91	Adiposis Dolorosa	16.9%
92	Alkalosis, Respiratory	16.9%
93	Alkaptonuria	16.7%
94	Glycogen Storage Disease	16.7%
95	Hypophosphatasia	16.7%
96	Insulin Resistance	16.7%
97	Osteoporosis, Postmenopausal	16.7%
98	Propionic acidemia	16.7%
99	Dihydropyrimidine Dehydrogenase Deficiency	16.7%
100	Cystinosis	16.7%
101	Renal tubular acidosis	16.3%
102	Fabry Disease	15.9%
103	Neuronal Ceroid-Lipofuscinoses	15.7%
104	Mitochondrial Myopathies	15.5%
105	Myelinolysis, Central Pontine	15.4%
106	Glycosuria	15.1%
107	Reye Syndrome	15.1%
108	Hepatic Encephalopathy	15%
109	Rickets	14.9%
110	Glycogen Storage Disease Type I	14.8%
111	Glycogen Storage Disease Type V	14.8%
112	Mucopolysaccharidosis III	14.6%
113	Child Nutrition Disorders	14.3%
114	Hypervitaminosis A	14.3%
115	Infant Nutrition Disorders	14.3%
116	Malnutrition	14.3%
117	MELAS Syndrome	14.1%
118	HIV-Associated Lipodystrophy Syndrome	14.1%
119	Adrenoleukodystrophy	13.7%
120	Zellweger Syndrome	13.5%
121	Menkes Kinky Hair Syndrome	13.3%
122	HIV Wasting Syndrome	13.3%
123	Gestational Diabetes	13%
124	Latent Autoimmune Diabetes in Adults	13%
125	Diabetes Mellitus, Experimental	12.8%
126	Osteomalacia	12.5%
127	Hepatolenticular Degeneration	12.4%
128	Porphyrias, Hepatic	12.3%
129	Cerebral Amyloid Angiopathy	12.3%
130	Wernicke Encephalopathy	12.2%
131	Glycosuria, Renal	12.2%
132	Refsum Disease	12.2%
133	Necrobiosis Lipoidica Diabeticorum	12.1%
134	Fanconi Anemia	11.9%
135	Deficiency Diseases	10.3%
136	Starvation	10.3%
137	Refeeding Syndrome	10.3%
138	Familial Periodic Paralysis	10.1%
139	Primary amyloidosis	10.1%
140	Variegate Porphyria	9.9%
141	Acute intermittent porphyria	9.9%
142	Porphyria Cutanea Tarda	9.9%
143	Friedreich Ataxia	9.9%
144	Renal Aminoacidurias	9.8%
145	Fanconi Syndrome	9.8%
146	Pseudohypoaldosteronism	9.8%
147	Liddle Syndrome	9.8%
148	Canavan Disease	9.8%
149	Alexander Disease	9.8%
150	Mucopolysaccharidosis II	9.7%
151	Sjogren-Larsson Syndrome	9.3%
152	Kearns-Sayre syndrome	9.3%
153	Hypokalemic periodic paralysis	8.9%
154	Frontotemporal dementia	8.8%
155	Cystinuria	8.8%
156	Kernicterus	8.7%
157	Cockayne Syndrome	8.6%
158	Kwashiorkor	8.5%
159	Magnesium Deficiency	8.5%
160	Potassium Deficiency	8.5%
161	Protein Deficiency	8.5%
162	Avitaminosis	8.5%
163	Gout	8.4%
164	Amyotrophic Lateral Sclerosis	8.4%
165	Antley-Bixler Syndrome Phenotype	8.2%
166	Renal Osteodystrophy	7.8%
167	Renal rickets	7.8%
168	Ataxia Telangiectasia	7.6%
169	Ascorbic Acid Deficiency	7.6%
170	Vitamin A Deficiency	7.6%
171	Vitamin D Deficiency	7.6%
172	Vitamin E Deficiency	7.6%
173	Marasmus	7.6%
174	Optic Atrophy, Hereditary, Leber	7.4%
175	Arthritis, Gouty	7.4%
176	Folic Acid Deficiency	7.1%
177	Pellagra	7.1%
178	Thiamine Deficiency	7.1%
179	Vitamin B 12 Deficiency	7.1%
180	Vitamin B 6 Deficiency	7.1%
181	Pyridoxine Deficiency	7.1%
182	Beriberi	6.9%
183	Xeroderma Pigmentosum	6.8%
184	Albinism	6.3%
185	Ichthyosis, X-Linked	5%
186	Anemia, Pernicious	4.5%
187	Obesity, Abdominal	4.1%
188	Obesity	3.9%
189	Vitamin K Deficiency	3.8%
190	Scurvy	3.5%
191	Pediatric Obesity	3.2%
192	Prader-Willi Syndrome	2.8%
193	Subacute Combined Degeneration	2.3%

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