MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Hemosiderosis

(UMLS:C0019114)

Definition:: Conditions in which there is a generalized increase in the iron stores of body tissues, particularly of liver and the MONONUCLEAR PHAGOCYTE SYSTEM, without demonstrable tissue damage. The name refers to the presence of stainable iron in the tissue in the form of hemosiderin.
UMLS ID:: C0019114
MeSH ID:: D006486

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.565.500.500

Synonym(s)

Hemosiderosis

HAEMOSIDEROSIS

HEMOSIDEROSIS

Haemosiderosis

Haemosiderosis, NOS

Hemosiderosis, NOS

haemosiderosis

hemosideroses

hemosiderosis

Associated Drug(s)

	Name	Reference(s)	Data Source
1	2-anisidine	28321044	CTD
2	3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone	8846998	CTD
3	4-chloronitrobenzene	3710033	CTD
4	4-nitroaniline	3710033	CTD
5	Amiodarone	18801087	CTD
6	Dapsone	17053738	CTD
7	Deferoxamine	6739047	CTD
8	Methotrexate	845977	CTD
9	Oxymetholone	4117807	CTD
10	Vitamin E	4214104	CTD
11	cresidine	12512871	CTD
12	cyclonite	21516383	CTD
13	propylene dichloride	2744274	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Acid-Base Imbalance	25.4%
2	Calcium Metabolism Disorders	25.4%
3	Phosphorus Metabolism Disorders	25.4%
4	Water-Electrolyte Imbalance	25.4%
5	Lipid Metabolism Disorders	25.4%
6	Mitochondrial Diseases	25.4%
7	Glucose Metabolism Disorders	25.4%
8	Wasting Syndrome	23%
9	Hypercalcemia	19.8%
10	Hypocalcemia	19.8%
11	Milk-Alkali Syndrome	19.8%
12	Osteopenia	17.2%
13	Brain Diseases, Metabolic	16.9%
14	Nutrition Disorders	16.4%
15	Lipodystrophy	14.9%
16	Acidosis	14.8%
17	Alkalosis	14.8%
18	Amyloidosis	14.8%
19	Calcinosis	14.8%
20	Hyperglycemia	14.8%
21	Hyperinsulinism	14.8%
22	Hyperkalemia	14.8%
23	Hypernatremia	14.8%
24	Hypoglycemia	14.8%
25	Hypokalemia	14.8%
26	Hyponatremia	14.8%
27	Xanthomatosis	14.8%
28	Hypophosphatemia	14.8%
29	Metabolic acidosis	14.8%
30	Dyslipidemias	14.8%
31	Xanthoma	14.8%
32	Pseudohypoparathyroidism	13.1%
33	Rickets	12.6%
34	Brain Diseases, Metabolic, Inborn	11.8%
35	Diabetes Mellitus	10.6%
36	Hyperhomocysteinemia	10.5%
37	Leigh Disease	10.3%
38	Dehydration	10.1%
39	Lipomatosis	10.1%
40	Water Intoxication	10.1%
41	Werner Syndrome	10.1%
42	Achlorhydria	9.9%
43	Amino Acid Metabolism, Inborn Errors	9.9%
44	Bloom Syndrome	9.9%
45	Carbohydrate Metabolism, Inborn Errors	9.9%
46	Metal Metabolism, Inborn Errors	9.9%
47	Osteoporosis	9.9%
48	Progeria	9.9%
49	Lysosomal Storage Diseases	9.9%
50	Bone Demineralization, Pathologic	9.9%
51	Cytochrome-c Oxidase Deficiency	9.9%
52	Peroxisomal Disorders	9.9%
53	Post-Traumatic Osteoporosis	9.9%
54	Celiac Disease	9.8%
55	Sprue, Tropical	9.8%
56	Steatorrhea	9.8%
57	Sprue	9.8%
58	Lactose Intolerance	9.7%
59	Acidosis, Lactic	9.7%
60	Calciphylaxis	9.7%
61	Hypolipoproteinemias	9.7%
62	Ketosis	9.7%
63	Ketonuria	9.7%
64	Ketoacidosis	9.7%
65	Ketonemia	9.7%
66	Vascular calcification	9.7%
67	Carbamoyl-Phosphate Synthase I Deficiency Disease	9%
68	Hyperlipoproteinemia Type IV	8.6%
69	Hyperlipoproteinemia Type V	8.6%
70	Diabetic Ketoacidosis	8.5%
71	Child Nutrition Disorders	8.5%
72	Hypervitaminosis A	8.5%
73	Infant Nutrition Disorders	8.5%
74	Malnutrition	8.5%
75	Hyperlipidemia, Familial Combined	8.4%
76	Osteomalacia	8.4%
77	Smith-Lemli-Opitz Syndrome	8.3%
78	Galactosemias	8.3%
79	Urea Cycle Disorders, Inborn	8.3%
80	Tyrosinemias	8.3%
81	Mitochondrial Encephalomyopathies	8.2%
82	Congenital Hyperinsulinism	8.1%
83	Hyperlipoproteinemia Type III	7.8%
84	Mitochondrial Myopathies	7.6%
85	Myelinolysis, Central Pontine	7.5%
86	Glycosuria	7.4%
87	Reye Syndrome	7.4%
88	Hepatic Encephalopathy	7.3%
89	Hyperphosphaturia	7.2%
90	Hypercholesterolemia	7.2%
91	Hyperlipoproteinemias	7.2%
92	Hypertriglyceridemia	7.2%
93	Hypoalphalipoproteinemias	7.2%
94	Familial Hypophosphatemic Rickets	6.8%
95	Homocystinuria	6.7%
96	HIV Wasting Syndrome	6.5%
97	Acidosis, Respiratory	6.5%
98	Adiposis Dolorosa	6.5%
99	Alkalosis, Respiratory	6.5%
100	Alkaptonuria	6.5%
101	Glycogen Storage Disease	6.5%
102	Hypophosphatasia	6.5%
103	Insulin Resistance	6.5%
104	Osteoporosis, Postmenopausal	6.5%
105	Propionic acidemia	6.5%
106	Dihydropyrimidine Dehydrogenase Deficiency	6.5%
107	Cystinosis	6.5%
108	Renal tubular acidosis	6.4%
109	Glycogen storage disease type II	6.4%
110	Gaucher Disease	6.2%
111	Amyloid Neuropathies, Familial	6.1%
112	Porphyrias, Hepatic	6%
113	Necrobiosis Lipoidica Diabeticorum	5.9%
114	Fanconi Anemia	5.8%
115	Nesidioblastosis	5.8%
116	Neuronal Ceroid-Lipofuscinoses	5.7%
117	HIV-Associated Lipodystrophy Syndrome	5.5%
118	Wernicke Encephalopathy	5.5%
119	Zellweger Syndrome	5.3%
120	Renal Osteodystrophy	5.3%
121	Renal rickets	5.3%
122	MELAS Syndrome	5.3%
123	Menkes Kinky Hair Syndrome	5.3%
124	Adrenoleukodystrophy	5.1%
125	Gestational Diabetes	5.1%
126	Latent Autoimmune Diabetes in Adults	5.1%
127	Tay-Sachs Disease	5.1%
128	Diabetes Mellitus, Experimental	5%
129	Niemann-Pick Disease, Type C	4.9%
130	Deficiency Diseases	4.9%
131	Starvation	4.9%
132	Refeeding Syndrome	4.9%
133	Hepatolenticular Degeneration	4.9%
134	Nephrocalcinosis	4.9%
135	Tetany	4.9%
136	Friedreich Ataxia	4.9%
137	Refsum Disease	4.8%
138	Glycosuria, Renal	4.8%
139	Cerebral Amyloid Angiopathy	4.8%
140	Glycogen Storage Disease Type I	4.8%
141	Glycogen Storage Disease Type V	4.8%
142	Mucopolysaccharidosis III	4.8%
143	Fabry Disease	4.8%
144	Kernicterus	4.3%
145	Cockayne Syndrome	4.2%
146	Familial Periodic Paralysis	4%
147	Primary amyloidosis	3.9%
148	Kearns-Sayre syndrome	3.9%
149	Variegate Porphyria	3.9%
150	Acute intermittent porphyria	3.9%
151	Porphyria Cutanea Tarda	3.9%
152	Renal Aminoacidurias	3.9%
153	Fanconi Syndrome	3.9%
154	Pseudohypoaldosteronism	3.9%
155	Liddle Syndrome	3.9%
156	Ataxia Telangiectasia	3.8%
157	Optic Atrophy, Hereditary, Leber	3.7%
158	Sjogren-Larsson Syndrome	3.4%
159	Xeroderma Pigmentosum	3.3%
160	Gout	3.3%
161	Amyotrophic Lateral Sclerosis	3.3%
162	Antley-Bixler Syndrome Phenotype	3.2%
163	Canavan Disease	3.2%
164	Alexander Disease	3.2%
165	Kwashiorkor	3.2%
166	Magnesium Deficiency	3.2%
167	Potassium Deficiency	3.2%
168	Protein Deficiency	3.2%
169	Avitaminosis	3.2%
170	Mucopolysaccharidosis II	3.2%
171	Hypokalemic periodic paralysis	2.9%
172	Frontotemporal dementia	2.9%
173	Cystinuria	2.9%
174	CREST Syndrome	2.8%
175	Albinism	2.5%
176	Arthritis, Gouty	2.4%
177	Ascorbic Acid Deficiency	2.4%
178	Vitamin A Deficiency	2.4%
179	Vitamin D Deficiency	2.4%
180	Vitamin E Deficiency	2.4%
181	Marasmus	2.4%
182	Folic Acid Deficiency	2%
183	Pellagra	2%
184	Thiamine Deficiency	2%
185	Vitamin B 12 Deficiency	2%
186	Vitamin B 6 Deficiency	2%
187	Pyridoxine Deficiency	2%
188	Ichthyosis, X-Linked	2%
189	Obesity	1.9%
190	Beriberi	1.8%
191	Obesity, Abdominal	1.6%
192	Pediatric Obesity	1.3%
193	Vitamin K Deficiency	1.2%
194	Anemia, Pernicious	1.2%
195	Prader-Willi Syndrome	1.1%
196	Scurvy	1%
197	Subacute Combined Degeneration	0.6%

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