MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Xanthoma

(UMLS:C0302314)

UMLS ID:: C0302314
MeSH ID:: D014973

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.584.750

Synonym(s)

Xanthoma

Deposition, xanthomatous

Xanthelasma

Xanthoma, NOS

Xanthomatous deposition

Xanthomatous deposition, NOS

clinical impressions xanthoma

xanthelasma

xanthelasmas

10.

xanthoma

11.

xanthomas

Associated Drug(s)

	Name	Number of Reports	Data Source
1	Olanzapine	FAERS: 10	US FAERS
2	Valproic Acid	FAERS: 6	US FAERS
3	BMS201038	FAERS: 2 Canada Vigilance: 1	Canada Vigilance SIDER US FAERS
4	Estradiol	FAERS: 2	US FAERS
5	Ibuprofen	FAERS: 2	US FAERS
6	Latanoprost	FAERS: 2	US FAERS
7	Stavudine	FAERS: 2	OFFSIDES US FAERS
8	Valproic Acid	FAERS: 2	US FAERS
9	pazopanib	FAERS: 2	US FAERS
10	Clobetasol	FAERS: 1	US FAERS
11	Minocycline	FAERS: 1	US FAERS
12	Mirtazapine	FAERS: 1	US FAERS
13	Rosuvastatin Calcium	FAERS: 1	US FAERS
14	Ruxolitinib phosphate	FAERS: 1	US FAERS
15	Warfarin	FAERS: 1	US FAERS
16	pasireotide	FAERS: 1	US FAERS
17	Amisulpride		OFFSIDES
18	Azathioprine		OFFSIDES
19	Biperiden		OFFSIDES
20	Captopril		OFFSIDES
21	Cholestyramine Resin		SIDER
22	Digoxin		OFFSIDES
23	Methylphenidate		OFFSIDES
24	Niacin		SIDER
25	Tretinoin		OFFSIDES
26	haloperidol decanoate		OFFSIDES
27	rofecoxib		OFFSIDES
28	zotepine		OFFSIDES

Similar ADE(s)

	Name	Semantic Similarity
1	Dyslipidemias	46.7%
2	Lipodystrophy	33.3%
3	Lipomatosis	31.8%
4	Acid-Base Imbalance	31%
5	Calcium Metabolism Disorders	31%
6	Iron Metabolism Disorders	31%
7	Phosphorus Metabolism Disorders	31%
8	Water-Electrolyte Imbalance	31%
9	Mitochondrial Diseases	31%
10	Glucose Metabolism Disorders	31%
11	Hypercholesterolemia	28.5%
12	Hyperlipoproteinemias	28.5%
13	Hypertriglyceridemia	28.5%
14	Wasting Syndrome	27.9%
15	Hypercalcemia	26.7%
16	Hypocalcemia	26.7%
17	Milk-Alkali Syndrome	26.7%
18	Hyperlipoproteinemia Type IV	26%
19	Hyperlipoproteinemia Type V	26%
20	Hypolipoproteinemias	24.4%
21	Adiposis Dolorosa	23.1%
22	Hyperlipidemia, Familial Combined	21.5%
23	Osteopenia	20.9%
24	Brain Diseases, Metabolic	20.5%
25	Hypoalphalipoproteinemias	20.1%
26	Acidosis	20%
27	Alkalosis	20%
28	Amyloidosis	20%
29	Calcinosis	20%
30	Hyperglycemia	20%
31	Hyperinsulinism	20%
32	Hyperkalemia	20%
33	Hyperlipoproteinemia Type III	20%
34	Hypernatremia	20%
35	Hypoglycemia	20%
36	Hypokalemia	20%
37	Hyponatremia	20%
38	Hypophosphatemia	20%
39	Metabolic acidosis	20%
40	Iron Overload	20%
41	Nutrition Disorders	18.5%
42	Smith-Lemli-Opitz Syndrome	18.1%
43	Pseudohypoparathyroidism	18.1%
44	Rickets	17.3%
45	Brain Diseases, Metabolic, Inborn	15.9%
46	Neuronal Ceroid-Lipofuscinoses	15.5%
47	Leigh Disease	15.2%
48	Hyperhomocysteinemia	15.1%
49	Acidosis, Lactic	14.8%
50	Calciphylaxis	14.8%
51	Hemosiderosis	14.8%
52	Ketosis	14.8%
53	Ketonuria	14.8%
54	Ketoacidosis	14.8%
55	Ketonemia	14.8%
56	Vascular calcification	14.8%
57	Diabetes Mellitus	14.3%
58	Gaucher Disease	14.1%
59	HIV-Associated Lipodystrophy Syndrome	13.9%
60	Carbamoyl-Phosphate Synthase I Deficiency Disease	13.8%
61	Lactose Intolerance	13.7%
62	Dehydration	13.6%
63	Water Intoxication	13.6%
64	Werner Syndrome	13.6%
65	Diabetic Ketoacidosis	13.5%
66	Achlorhydria	13.3%
67	Amino Acid Metabolism, Inborn Errors	13.3%
68	Bloom Syndrome	13.3%
69	Carbohydrate Metabolism, Inborn Errors	13.3%
70	Metal Metabolism, Inborn Errors	13.3%
71	Osteoporosis	13.3%
72	Progeria	13.3%
73	Lysosomal Storage Diseases	13.3%
74	Bone Demineralization, Pathologic	13.3%
75	Cytochrome-c Oxidase Deficiency	13.3%
76	Peroxisomal Disorders	13.3%
77	Post-Traumatic Osteoporosis	13.3%
78	Celiac Disease	13.2%
79	Sprue, Tropical	13.2%
80	Steatorrhea	13.2%
81	Sprue	13.2%
82	Osteomalacia	13%
83	Tay-Sachs Disease	12.5%
84	Galactosemias	12.5%
85	Urea Cycle Disorders, Inborn	12.5%
86	Tyrosinemias	12.5%
87	Congenital Hyperinsulinism	12.2%
88	Niemann-Pick Disease, Type C	11.8%
89	Familial Hypophosphatemic Rickets	11.5%
90	Mitochondrial Encephalomyopathies	11.5%
91	Hyperphosphaturia	10.9%
92	Fabry Disease	10.9%
93	Glycogen storage disease type II	10.6%
94	Homocystinuria	10.4%
95	Child Nutrition Disorders	10.3%
96	Hypervitaminosis A	10.3%
97	Infant Nutrition Disorders	10.3%
98	Malnutrition	10.3%
99	Mitochondrial Myopathies	10.2%
100	Myelinolysis, Central Pontine	10.1%
101	Glycosuria	9.9%
102	Reye Syndrome	9.9%
103	Acidosis, Respiratory	9.9%
104	Alkalosis, Respiratory	9.9%
105	Hepatic Encephalopathy	9.8%
106	Nesidioblastosis	9.8%
107	Alkaptonuria	9.8%
108	Glycogen Storage Disease	9.8%
109	Hypophosphatasia	9.8%
110	Insulin Resistance	9.8%
111	Osteoporosis, Postmenopausal	9.8%
112	Propionic acidemia	9.8%
113	Dihydropyrimidine Dehydrogenase Deficiency	9.8%
114	Cystinosis	9.8%
115	Amyloid Neuropathies, Familial	9.8%
116	Renal tubular acidosis	9.7%
117	Sjogren-Larsson Syndrome	9.3%
118	HIV Wasting Syndrome	8.8%
119	MELAS Syndrome	8.2%
120	Renal Osteodystrophy	8.2%
121	Renal rickets	8.2%
122	Porphyrias, Hepatic	8.1%
123	Glycogen Storage Disease Type I	8.1%
124	Glycogen Storage Disease Type V	8.1%
125	Zellweger Syndrome	8%
126	Mucopolysaccharidosis III	8%
127	Adrenoleukodystrophy	8%
128	Necrobiosis Lipoidica Diabeticorum	7.9%
129	Menkes Kinky Hair Syndrome	7.9%
130	Fanconi Anemia	7.8%
131	Wernicke Encephalopathy	7.7%
132	Gestational Diabetes	7.7%
133	Latent Autoimmune Diabetes in Adults	7.7%
134	Diabetes Mellitus, Experimental	7.6%
135	Hepatolenticular Degeneration	7.4%
136	Nephrocalcinosis	7.4%
137	Tetany	7.4%
138	Refsum Disease	7.3%
139	Glycosuria, Renal	7.3%
140	Cerebral Amyloid Angiopathy	7.2%
141	Deficiency Diseases	6.7%
142	Starvation	6.7%
143	Refeeding Syndrome	6.7%
144	Friedreich Ataxia	6.5%
145	Familial Periodic Paralysis	6%
146	Primary amyloidosis	6%
147	Variegate Porphyria	5.9%
148	Acute intermittent porphyria	5.9%
149	Porphyria Cutanea Tarda	5.9%
150	Renal Aminoacidurias	5.8%
151	Fanconi Syndrome	5.8%
152	Pseudohypoaldosteronism	5.8%
153	Liddle Syndrome	5.8%
154	Kernicterus	5.7%
155	Kearns-Sayre syndrome	5.7%
156	Cockayne Syndrome	5.7%
157	Canavan Disease	5.4%
158	Alexander Disease	5.4%
159	Mucopolysaccharidosis II	5.3%
160	Ataxia Telangiectasia	5.1%
161	Gout	5%
162	Amyotrophic Lateral Sclerosis	5%
163	Kwashiorkor	4.9%
164	Magnesium Deficiency	4.9%
165	Potassium Deficiency	4.9%
166	Protein Deficiency	4.9%
167	Avitaminosis	4.9%
168	Optic Atrophy, Hereditary, Leber	4.9%
169	Antley-Bixler Syndrome Phenotype	4.9%
170	Hypokalemic periodic paralysis	4.9%
171	Frontotemporal dementia	4.8%
172	Cystinuria	4.8%
173	Xeroderma Pigmentosum	4.5%
174	CREST Syndrome	4.2%
175	Ascorbic Acid Deficiency	4.1%
176	Vitamin A Deficiency	4.1%
177	Vitamin D Deficiency	4.1%
178	Vitamin E Deficiency	4.1%
179	Marasmus	4.1%
180	Arthritis, Gouty	4.1%
181	Albinism	3.7%
182	Folic Acid Deficiency	3.6%
183	Pellagra	3.6%
184	Thiamine Deficiency	3.6%
185	Vitamin B 12 Deficiency	3.6%
186	Vitamin B 6 Deficiency	3.6%
187	Pyridoxine Deficiency	3.6%
188	Beriberi	3.4%
189	Ichthyosis, X-Linked	3%
190	Obesity	2.6%
191	Obesity, Abdominal	2.4%
192	Anemia, Pernicious	2.3%
193	Vitamin K Deficiency	2.1%
194	Pediatric Obesity	1.9%
195	Scurvy	1.8%
196	Prader-Willi Syndrome	1.6%
197	Subacute Combined Degeneration	1.2%

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