MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Hyperlipoproteinemias

(UMLS:C0020476)

Definition:: Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation.
UMLS ID:: C0020476
MeSH ID:: D006951

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.584.500.500.644

Synonym(s)

Hyperlipoproteinemias

HYPERLIPOPROTEINEMIA

Hyperlipoproteinaemia, NOS

Hyperlipoproteinemia

Hyperlipoproteinemia, NOS

hyperlipidemia

hyperlipoproteinaemia

hyperlipoproteinaemias

hyperlipoproteinemia

10.

hyperlipoproteinemias

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Atorvastatin	12633795 12842237 19240310	CTD
2	Bezafibrate	2360915 2722079	CTD
3	Chlorogenic Acid	20696151	CTD
4	Cholesterol	17611329	CTD
5	Clofibrate	7080553 7157849	CTD
6	Danazol	15806011	CTD
7	Etretinate	3721869	CTD
8	Ezetimibe	20377808	CTD
9	Fenofibrate	20855072	CTD
10	Isotretinoin	3721869	CTD
11	Niacinamide	20696151	CTD
12	Niacin	View details 11498460 15342288 17425952 17611329 19240310 20377808 20831686 20855072	CTD
13	Puromycin Aminonucleoside	7595070	CTD
14	Riboflavin	17425952	CTD
15	Rosuvastatin Calcium	16860175 20831686	CTD
16	Simvastatin	View details 10195365 11498460 12633795 20377808	CTD
17	Streptozocin	20696151	CTD
18	Tamoxifen	17425952	CTD
19	Ubiquinone	17425952	CTD
20	cobaltiprotoporphyrin	22193921	CTD
21	potassium bromate	26296324	CTD
22	tetrahydrocurcumin	20696151	CTD
23	vanillin	26296324	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Hypercholesterolemia	49.2%
2	Hypertriglyceridemia	49.2%
3	Xanthomatosis	28.5%
4	Xanthoma	28.5%
5	Hyperlipidemia, Familial Combined	28.4%
6	Acid-Base Imbalance	22.7%
7	Calcium Metabolism Disorders	22.7%
8	Iron Metabolism Disorders	22.7%
9	Phosphorus Metabolism Disorders	22.7%
10	Water-Electrolyte Imbalance	22.7%
11	Mitochondrial Diseases	22.7%
12	Glucose Metabolism Disorders	22.7%
13	Hypolipoproteinemias	21.7%
14	Lipodystrophy	20.6%
15	Wasting Syndrome	20.6%
16	Lipomatosis	19.6%
17	Hyperlipoproteinemia Type IV	17.7%
18	Hyperlipoproteinemia Type V	17.7%
19	Hypercalcemia	16.4%
20	Hypocalcemia	16.4%
21	Milk-Alkali Syndrome	16.4%
22	Osteopenia	15.4%
23	Nutrition Disorders	15.3%
24	Brain Diseases, Metabolic	15.1%
25	Smith-Lemli-Opitz Syndrome	14.5%
26	Hypoalphalipoproteinemias	14.3%
27	Acidosis	12.2%
28	Alkalosis	12.2%
29	Amyloidosis	12.2%
30	Calcinosis	12.2%
31	Hyperglycemia	12.2%
32	Hyperinsulinism	12.2%
33	Hyperkalemia	12.2%
34	Hypernatremia	12.2%
35	Hypoglycemia	12.2%
36	Hypokalemia	12.2%
37	Hyponatremia	12.2%
38	Hypophosphatemia	12.2%
39	Metabolic acidosis	12.2%
40	Iron Overload	12.2%
41	Adiposis Dolorosa	11.4%
42	Pseudohypoparathyroidism	10.6%
43	Rickets	10.3%
44	Brain Diseases, Metabolic, Inborn	9.8%
45	Diabetes Mellitus	8.8%
46	Dehydration	8.4%
47	Water Intoxication	8.4%
48	Werner Syndrome	8.4%
49	Hyperhomocysteinemia	8.2%
50	Achlorhydria	8.2%
51	Amino Acid Metabolism, Inborn Errors	8.2%
52	Bloom Syndrome	8.2%
53	Carbohydrate Metabolism, Inborn Errors	8.2%
54	Metal Metabolism, Inborn Errors	8.2%
55	Osteoporosis	8.2%
56	Progeria	8.2%
57	Lysosomal Storage Diseases	8.2%
58	Bone Demineralization, Pathologic	8.2%
59	Cytochrome-c Oxidase Deficiency	8.2%
60	Peroxisomal Disorders	8.2%
61	Post-Traumatic Osteoporosis	8.2%
62	Celiac Disease	8.1%
63	Sprue, Tropical	8.1%
64	Steatorrhea	8.1%
65	Sprue	8.1%
66	Leigh Disease	7.8%
67	Lactose Intolerance	7.8%
68	Child Nutrition Disorders	7.6%
69	Hypervitaminosis A	7.6%
70	Infant Nutrition Disorders	7.6%
71	Malnutrition	7.6%
72	Neuronal Ceroid-Lipofuscinoses	7.3%
73	Acidosis, Lactic	7.2%
74	Calciphylaxis	7.2%
75	Hemosiderosis	7.2%
76	Ketosis	7.2%
77	Ketonuria	7.2%
78	Ketoacidosis	7.2%
79	Ketonemia	7.2%
80	Vascular calcification	7.2%
81	HIV-Associated Lipodystrophy Syndrome	6.9%
82	Carbamoyl-Phosphate Synthase I Deficiency Disease	6.6%
83	Mitochondrial Encephalomyopathies	6.5%
84	Mitochondrial Myopathies	6.3%
85	Myelinolysis, Central Pontine	6.2%
86	Galactosemias	6.2%
87	Urea Cycle Disorders, Inborn	6.2%
88	Tyrosinemias	6.2%
89	Osteomalacia	6.2%
90	Glycosuria	6.1%
91	Reye Syndrome	6.1%
92	Hepatic Encephalopathy	6.1%
93	Diabetic Ketoacidosis	6%
94	Congenital Hyperinsulinism	6%
95	HIV Wasting Syndrome	5.4%
96	Hyperphosphaturia	5.4%
97	Gaucher Disease	5%
98	Porphyrias, Hepatic	5%
99	Necrobiosis Lipoidica Diabeticorum	4.9%
100	Acidosis, Respiratory	4.9%
101	Alkalosis, Respiratory	4.9%
102	Homocystinuria	4.9%
103	Fanconi Anemia	4.9%
104	Renal tubular acidosis	4.8%
105	Alkaptonuria	4.8%
106	Glycogen Storage Disease	4.8%
107	Hypophosphatasia	4.8%
108	Insulin Resistance	4.8%
109	Osteoporosis, Postmenopausal	4.8%
110	Propionic acidemia	4.8%
111	Dihydropyrimidine Dehydrogenase Deficiency	4.8%
112	Cystinosis	4.8%
113	Familial Hypophosphatemic Rickets	4.5%
114	Wernicke Encephalopathy	4.4%
115	Sjogren-Larsson Syndrome	4.4%
116	Amyloid Neuropathies, Familial	4.2%
117	Glycogen storage disease type II	4.2%
118	Deficiency Diseases	4.1%
119	Starvation	4.1%
120	Refeeding Syndrome	4.1%
121	Friedreich Ataxia	4%
122	Zellweger Syndrome	4%
123	Menkes Kinky Hair Syndrome	4%
124	Fabry Disease	3.9%
125	Nesidioblastosis	3.9%
126	Renal Osteodystrophy	3.9%
127	Renal rickets	3.9%
128	MELAS Syndrome	3.8%
129	Gestational Diabetes	3.8%
130	Latent Autoimmune Diabetes in Adults	3.8%
131	Diabetes Mellitus, Experimental	3.7%
132	Adrenoleukodystrophy	3.7%
133	Hepatolenticular Degeneration	3.7%
134	Niemann-Pick Disease, Type C	3.6%
135	Nephrocalcinosis	3.6%
136	Tetany	3.6%
137	Refsum Disease	3.6%
138	Glycosuria, Renal	3.6%
139	Hyperlipoproteinemia Type III	3.6%
140	Cerebral Amyloid Angiopathy	3.6%
141	Kernicterus	3.6%
142	Cockayne Syndrome	3.5%
143	Tay-Sachs Disease	3.5%
144	Mucopolysaccharidosis III	3.2%
145	Glycogen Storage Disease Type I	3.2%
146	Glycogen Storage Disease Type V	3.2%
147	Ataxia Telangiectasia	3.1%
148	Kearns-Sayre syndrome	3.1%
149	Optic Atrophy, Hereditary, Leber	3%
150	Familial Periodic Paralysis	3%
151	Primary amyloidosis	3%
152	Variegate Porphyria	2.9%
153	Acute intermittent porphyria	2.9%
154	Porphyria Cutanea Tarda	2.9%
155	Renal Aminoacidurias	2.9%
156	Fanconi Syndrome	2.9%
157	Pseudohypoaldosteronism	2.9%
158	Liddle Syndrome	2.9%
159	Xeroderma Pigmentosum	2.8%
160	Gout	2.5%
161	Amyotrophic Lateral Sclerosis	2.5%
162	Antley-Bixler Syndrome Phenotype	2.4%
163	Kwashiorkor	2.4%
164	Magnesium Deficiency	2.4%
165	Potassium Deficiency	2.4%
166	Protein Deficiency	2.4%
167	Avitaminosis	2.4%
168	Canavan Disease	2.1%
169	Alexander Disease	2.1%
170	Mucopolysaccharidosis II	2.1%
171	CREST Syndrome	2.1%
172	Hypokalemic periodic paralysis	1.9%
173	Frontotemporal dementia	1.9%
174	Cystinuria	1.9%
175	Albinism	1.9%
176	Arthritis, Gouty	1.6%
177	Obesity	1.6%
178	Ascorbic Acid Deficiency	1.6%
179	Vitamin A Deficiency	1.6%
180	Vitamin D Deficiency	1.6%
181	Vitamin E Deficiency	1.6%
182	Marasmus	1.6%
183	Ichthyosis, X-Linked	1.5%
184	Obesity, Abdominal	1.2%
185	Folic Acid Deficiency	1.2%
186	Pellagra	1.2%
187	Thiamine Deficiency	1.2%
188	Vitamin B 12 Deficiency	1.2%
189	Vitamin B 6 Deficiency	1.2%
190	Pyridoxine Deficiency	1.2%
191	Beriberi	1%
192	Pediatric Obesity	1%
193	Prader-Willi Syndrome	0.8%
194	Vitamin K Deficiency	0.8%
195	Anemia, Pernicious	0.7%
196	Scurvy	0.6%
197	Subacute Combined Degeneration	0.3%

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