MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Iron Metabolism Disorders

(UMLS:C0012715)

Definition:: Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. (From Mosby's Medical, Nursing, & Allied Health Dictionary, 4th ed)
UMLS ID:: C0012715
MeSH ID:: D019189

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.565

Synonym(s)

Iron Metabolism Disorders

Disorder of iron metabolism

Disorder of iron metabolism, NOS

Disorder of iron metabolism, unspecified

Disorders of iron metabolism

Iron metabolism disorder

Iron--Metabolism--Disorders

disorder of iron metabolism

disorders iron

10.

disorders iron metabolism

11.

disorders of iron metabolism

12.

iron disorder

13.

iron metabolism disorder

14.

iron; metabolic disorder

15.

metabolic disorder; iron

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Manganese Compounds		21458486	CTD
2	chromium hexavalent ion		24418189	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Acid-Base Imbalance	42.9%
2	Calcium 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	Hypercalcemia	40.9%
9	Hypocalcemia	40.9%
10	Milk-Alkali Syndrome	40.9%
11	Wasting Syndrome	38.1%
12	Acidosis	31%
13	Alkalosis	31%
14	Amyloidosis	31%
15	Calcinosis	31%
16	Hyperglycemia	31%
17	Hyperinsulinism	31%
18	Hyperkalemia	31%
19	Hypernatremia	31%
20	Hypoglycemia	31%
21	Hypokalemia	31%
22	Hyponatremia	31%
23	Xanthomatosis	31%
24	Hypophosphatemia	31%
25	Metabolic acidosis	31%
26	Dyslipidemias	31%
27	Xanthoma	31%
28	Lipodystrophy	30.5%
29	Osteopenia	28.6%
30	Pseudohypoparathyroidism	28.3%
31	Brain Diseases, Metabolic	27.9%
32	Rickets	26.9%
33	Hyperlipoproteinemia Type IV	26.4%
34	Hyperlipoproteinemia Type V	26.4%
35	Acidosis, Lactic	25.4%
36	Calciphylaxis	25.4%
37	Ketosis	25.4%
38	Ketonuria	25.4%
39	Ketoacidosis	25.4%
40	Ketonemia	25.4%
41	Vascular calcification	25.4%
42	Leigh Disease	25.1%
43	Hypolipoproteinemias	24.8%
44	Hyperhomocysteinemia	24.5%
45	Brain Diseases, Metabolic, Inborn	24.2%
46	Carbamoyl-Phosphate Synthase I Deficiency Disease	23.7%
47	Diabetic Ketoacidosis	23.7%
48	Hyperlipidemia, Familial Combined	23.5%
49	Nutrition Disorders	23.1%
50	Hyperlipoproteinemia Type III	22.8%
51	Hypercholesterolemia	22.7%
52	Hyperlipoproteinemias	22.7%
53	Hypertriglyceridemia	22.7%
54	Osteomalacia	22.3%
55	Hypoalphalipoproteinemias	22%
56	Diabetes Mellitus	22%
57	Lactose Intolerance	21.9%
58	Smith-Lemli-Opitz Syndrome	21.1%
59	Galactosemias	21%
60	Urea Cycle Disorders, Inborn	21%
61	Tyrosinemias	21%
62	Dehydration	20.9%
63	Lipomatosis	20.9%
64	Water Intoxication	20.9%
65	Werner Syndrome	20.9%
66	Familial Hypophosphatemic Rickets	20.9%
67	Gaucher Disease	20.6%
68	Congenital Hyperinsulinism	20.5%
69	Achlorhydria	20.5%
70	Amino Acid Metabolism, Inborn Errors	20.5%
71	Bloom Syndrome	20.5%
72	Carbohydrate Metabolism, Inborn Errors	20.5%
73	Metal Metabolism, Inborn Errors	20.5%
74	Osteoporosis	20.5%
75	Progeria	20.5%
76	Lysosomal Storage Diseases	20.5%
77	Bone Demineralization, Pathologic	20.5%
78	Cytochrome-c Oxidase Deficiency	20.5%
79	Peroxisomal Disorders	20.5%
80	Post-Traumatic Osteoporosis	20.5%
81	Celiac Disease	20.2%
82	Sprue, Tropical	20.2%
83	Steatorrhea	20.2%
84	Sprue	20.2%
85	Tay-Sachs Disease	19.4%
86	Glycogen storage disease type II	19.3%
87	Hyperphosphaturia	18.3%
88	Mitochondrial Encephalomyopathies	18.2%
89	Niemann-Pick Disease, Type C	18%
90	Nesidioblastosis	17.9%
91	Homocystinuria	17.9%
92	Amyloid Neuropathies, Familial	17.2%
93	Acidosis, Respiratory	16.9%
94	Adiposis Dolorosa	16.9%
95	Alkalosis, Respiratory	16.9%
96	Alkaptonuria	16.7%
97	Glycogen Storage Disease	16.7%
98	Hypophosphatasia	16.7%
99	Insulin Resistance	16.7%
100	Osteoporosis, Postmenopausal	16.7%
101	Propionic acidemia	16.7%
102	Dihydropyrimidine Dehydrogenase Deficiency	16.7%
103	Cystinosis	16.7%
104	Renal tubular acidosis	16.3%
105	Fabry Disease	15.9%
106	Neuronal Ceroid-Lipofuscinoses	15.7%
107	Mitochondrial Myopathies	15.5%
108	Myelinolysis, Central Pontine	15.4%
109	Glycosuria	15.1%
110	Reye Syndrome	15.1%
111	Hepatic Encephalopathy	15%
112	Glycogen Storage Disease Type I	14.8%
113	Glycogen Storage Disease Type V	14.8%
114	Mucopolysaccharidosis III	14.6%
115	Child Nutrition Disorders	14.3%
116	Hypervitaminosis A	14.3%
117	Infant Nutrition Disorders	14.3%
118	Malnutrition	14.3%
119	MELAS Syndrome	14.1%
120	HIV-Associated Lipodystrophy Syndrome	14.1%
121	Renal Osteodystrophy	13.9%
122	Renal rickets	13.9%
123	Adrenoleukodystrophy	13.7%
124	Zellweger Syndrome	13.5%
125	Menkes Kinky Hair Syndrome	13.3%
126	HIV Wasting Syndrome	13.3%
127	Gestational Diabetes	13%
128	Latent Autoimmune Diabetes in Adults	13%
129	Diabetes Mellitus, Experimental	12.8%
130	Nephrocalcinosis	12.5%
131	Tetany	12.5%
132	Hepatolenticular Degeneration	12.4%
133	Porphyrias, Hepatic	12.3%
134	Cerebral Amyloid Angiopathy	12.3%
135	Wernicke Encephalopathy	12.2%
136	Glycosuria, Renal	12.2%
137	Refsum Disease	12.2%
138	Necrobiosis Lipoidica Diabeticorum	12.1%
139	Fanconi Anemia	11.9%
140	Deficiency Diseases	10.3%
141	Starvation	10.3%
142	Refeeding Syndrome	10.3%
143	Familial Periodic Paralysis	10.1%
144	Primary amyloidosis	10.1%
145	Variegate Porphyria	9.9%
146	Acute intermittent porphyria	9.9%
147	Porphyria Cutanea Tarda	9.9%
148	Friedreich Ataxia	9.9%
149	Renal Aminoacidurias	9.8%
150	Fanconi Syndrome	9.8%
151	Pseudohypoaldosteronism	9.8%
152	Liddle Syndrome	9.8%
153	Canavan Disease	9.8%
154	Alexander Disease	9.8%
155	Mucopolysaccharidosis II	9.7%
156	Sjogren-Larsson Syndrome	9.3%
157	Kearns-Sayre syndrome	9.3%
158	Hypokalemic periodic paralysis	8.9%
159	Frontotemporal dementia	8.8%
160	Cystinuria	8.8%
161	Kernicterus	8.7%
162	Cockayne Syndrome	8.6%
163	Kwashiorkor	8.5%
164	Magnesium Deficiency	8.5%
165	Potassium Deficiency	8.5%
166	Protein Deficiency	8.5%
167	Avitaminosis	8.5%
168	Gout	8.4%
169	Amyotrophic Lateral Sclerosis	8.4%
170	Antley-Bixler Syndrome Phenotype	8.2%
171	Ataxia Telangiectasia	7.6%
172	Ascorbic Acid Deficiency	7.6%
173	Vitamin A Deficiency	7.6%
174	Vitamin D Deficiency	7.6%
175	Vitamin E Deficiency	7.6%
176	Marasmus	7.6%
177	Optic Atrophy, Hereditary, Leber	7.4%
178	Arthritis, Gouty	7.4%
179	Folic Acid Deficiency	7.1%
180	Pellagra	7.1%
181	Thiamine Deficiency	7.1%
182	Vitamin B 12 Deficiency	7.1%
183	Vitamin B 6 Deficiency	7.1%
184	Pyridoxine Deficiency	7.1%
185	CREST Syndrome	7%
186	Beriberi	6.9%
187	Xeroderma Pigmentosum	6.8%
188	Albinism	6.3%
189	Ichthyosis, X-Linked	5%
190	Anemia, Pernicious	4.5%
191	Obesity, Abdominal	4.1%
192	Obesity	3.9%
193	Vitamin K Deficiency	3.8%
194	Scurvy	3.5%
195	Pediatric Obesity	3.2%
196	Prader-Willi Syndrome	2.8%
197	Subacute Combined Degeneration	2.3%

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