MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Lipid Metabolism Disorders

(UMLS:C0154251)

Definition:: Pathological conditions resulting from abnormal anabolism or catabolism of lipids in the body.
UMLS ID:: C0154251
MeSH ID:: D052439

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.584

Synonym(s)

Lipid Metabolism Disorders

Disease of lipid metabolism

Disease;lipid metabolism

Disorder of Lipid Metabolism

Disorder of lipid metabolism

Disorder;lipid metabolism

LIPID METABOLISM DISORDER NOS

Lipid Metabolism Disorder

Lipid disorder

10.

Lipid metabolism disorder

11.

Lipids--Metabolism--Disorders

12.

Unspecified disorder of lipoid metabolism

13.

disorder lipid metabolism

14.

disorder; lipid metabolism

15.

disorders fat

16.

disorders fats

17.

disorders lipid

18.

disorders lipids

19.

fat disorder

20.

lipid disorder

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Aflatoxin B1	23385219	CTD
2	Triiodothyronine	6816881	CTD
3	carbendazim	30496565	CTD
4	perhexiline maleate	68353	CTD
5	pirinixic acid	20614104	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Acid-Base Imbalance	42.9%
2	Calcium Metabolism Disorders	42.9%
3	Iron Metabolism Disorders	42.9%
4	Phosphorus Metabolism Disorders	42.9%
5	Water-Electrolyte Imbalance	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	Hypophosphatemia	31%
24	Metabolic acidosis	31%
25	Iron Overload	31%
26	Osteopenia	28.6%
27	Pseudohypoparathyroidism	28.3%
28	Brain Diseases, Metabolic	27.9%
29	Rickets	26.9%
30	Acidosis, Lactic	25.4%
31	Calciphylaxis	25.4%
32	Hemosiderosis	25.4%
33	Ketosis	25.4%
34	Ketonuria	25.4%
35	Ketoacidosis	25.4%
36	Ketonemia	25.4%
37	Vascular calcification	25.4%
38	Leigh Disease	25.1%
39	Hyperhomocysteinemia	24.5%
40	Brain Diseases, Metabolic, Inborn	24.2%
41	Carbamoyl-Phosphate Synthase I Deficiency Disease	23.7%
42	Diabetic Ketoacidosis	23.7%
43	Nutrition Disorders	23.1%
44	Osteomalacia	22.3%
45	Diabetes Mellitus	22%
46	Lactose Intolerance	21.9%
47	Galactosemias	21%
48	Urea Cycle Disorders, Inborn	21%
49	Tyrosinemias	21%
50	Dehydration	20.9%
51	Water Intoxication	20.9%
52	Werner Syndrome	20.9%
53	Familial Hypophosphatemic Rickets	20.9%
54	Congenital Hyperinsulinism	20.5%
55	Achlorhydria	20.5%
56	Amino Acid Metabolism, Inborn Errors	20.5%
57	Bloom Syndrome	20.5%
58	Carbohydrate Metabolism, Inborn Errors	20.5%
59	Metal Metabolism, Inborn Errors	20.5%
60	Osteoporosis	20.5%
61	Progeria	20.5%
62	Lysosomal Storage Diseases	20.5%
63	Bone Demineralization, Pathologic	20.5%
64	Cytochrome-c Oxidase Deficiency	20.5%
65	Peroxisomal Disorders	20.5%
66	Post-Traumatic Osteoporosis	20.5%
67	Celiac Disease	20.2%
68	Sprue, Tropical	20.2%
69	Steatorrhea	20.2%
70	Sprue	20.2%
71	Glycogen storage disease type II	19.3%
72	Hyperphosphaturia	18.3%
73	Mitochondrial Encephalomyopathies	18.2%
74	Nesidioblastosis	17.9%
75	Homocystinuria	17.9%
76	Amyloid Neuropathies, Familial	17.2%
77	Acidosis, Respiratory	16.9%
78	Alkalosis, Respiratory	16.9%
79	Alkaptonuria	16.7%
80	Glycogen Storage Disease	16.7%
81	Hypophosphatasia	16.7%
82	Insulin Resistance	16.7%
83	Osteoporosis, Postmenopausal	16.7%
84	Propionic acidemia	16.7%
85	Dihydropyrimidine Dehydrogenase Deficiency	16.7%
86	Cystinosis	16.7%
87	Renal tubular acidosis	16.3%
88	Gaucher Disease	16.3%
89	Mitochondrial Myopathies	15.5%
90	Tay-Sachs Disease	15.5%
91	Myelinolysis, Central Pontine	15.4%
92	Lipodystrophy	15.3%
93	Glycosuria	15.1%
94	Reye Syndrome	15.1%
95	Hepatic Encephalopathy	15%
96	Glycogen Storage Disease Type I	14.8%
97	Glycogen Storage Disease Type V	14.8%
98	Mucopolysaccharidosis III	14.6%
99	Niemann-Pick Disease, Type C	14.3%
100	Child Nutrition Disorders	14.3%
101	Hypervitaminosis A	14.3%
102	Infant Nutrition Disorders	14.3%
103	Malnutrition	14.3%
104	Smith-Lemli-Opitz Syndrome	14.1%
105	MELAS Syndrome	14.1%
106	Renal Osteodystrophy	13.9%
107	Renal rickets	13.9%
108	Adrenoleukodystrophy	13.7%
109	Zellweger Syndrome	13.5%
110	Menkes Kinky Hair Syndrome	13.3%
111	HIV Wasting Syndrome	13.3%
112	Gestational Diabetes	13%
113	Latent Autoimmune Diabetes in Adults	13%
114	Diabetes Mellitus, Experimental	12.8%
115	Fabry Disease	12.6%
116	Nephrocalcinosis	12.5%
117	Tetany	12.5%
118	Hypolipoproteinemias	12.4%
119	Hepatolenticular Degeneration	12.4%
120	Hyperlipidemia, Familial Combined	12.3%
121	Porphyrias, Hepatic	12.3%
122	Hyperlipoproteinemia Type III	12.3%
123	Cerebral Amyloid Angiopathy	12.3%
124	Wernicke Encephalopathy	12.2%
125	Glycosuria, Renal	12.2%
126	Refsum Disease	12.2%
127	Necrobiosis Lipoidica Diabeticorum	12.1%
128	Fanconi Anemia	11.9%
129	Hypoalphalipoproteinemias	11%
130	Deficiency Diseases	10.3%
131	Starvation	10.3%
132	Refeeding Syndrome	10.3%
133	Familial Periodic Paralysis	10.1%
134	Primary amyloidosis	10.1%
135	Variegate Porphyria	9.9%
136	Acute intermittent porphyria	9.9%
137	Porphyria Cutanea Tarda	9.9%
138	Friedreich Ataxia	9.9%
139	Renal Aminoacidurias	9.8%
140	Fanconi Syndrome	9.8%
141	Pseudohypoaldosteronism	9.8%
142	Liddle Syndrome	9.8%
143	Canavan Disease	9.8%
144	Alexander Disease	9.8%
145	Hyperlipoproteinemia Type IV	9.8%
146	Hyperlipoproteinemia Type V	9.8%
147	Mucopolysaccharidosis II	9.7%
148	Kearns-Sayre syndrome	9.3%
149	Hypokalemic periodic paralysis	8.9%
150	Frontotemporal dementia	8.8%
151	Cystinuria	8.8%
152	Kernicterus	8.7%
153	Cockayne Syndrome	8.6%
154	Kwashiorkor	8.5%
155	Magnesium Deficiency	8.5%
156	Potassium Deficiency	8.5%
157	Protein Deficiency	8.5%
158	Avitaminosis	8.5%
159	Gout	8.4%
160	Amyotrophic Lateral Sclerosis	8.4%
161	Antley-Bixler Syndrome Phenotype	8.2%
162	Ataxia Telangiectasia	7.6%
163	Ascorbic Acid Deficiency	7.6%
164	Vitamin A Deficiency	7.6%
165	Vitamin D Deficiency	7.6%
166	Vitamin E Deficiency	7.6%
167	Marasmus	7.6%
168	Neuronal Ceroid-Lipofuscinoses	7.4%
169	Optic Atrophy, Hereditary, Leber	7.4%
170	Arthritis, Gouty	7.4%
171	Folic Acid Deficiency	7.1%
172	Pellagra	7.1%
173	Thiamine Deficiency	7.1%
174	Vitamin B 12 Deficiency	7.1%
175	Vitamin B 6 Deficiency	7.1%
176	Pyridoxine Deficiency	7.1%
177	CREST Syndrome	7%
178	HIV-Associated Lipodystrophy Syndrome	7%
179	Beriberi	6.9%
180	Xeroderma Pigmentosum	6.8%
181	Albinism	6.3%
182	Ichthyosis, X-Linked	5%
183	Anemia, Pernicious	4.5%
184	Sjogren-Larsson Syndrome	4.4%
185	Obesity, Abdominal	4.1%
186	Obesity	3.9%
187	Vitamin K Deficiency	3.8%
188	Scurvy	3.5%
189	Pediatric Obesity	3.2%
190	Prader-Willi Syndrome	2.8%
191	Subacute Combined Degeneration	2.3%

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