MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Obesity, Abdominal

(UMLS:C0311277)

Definition:: A condition of having excess fat in the abdomen. Abdominal obesity is typically defined as waist circumferences of 40 inches or more in men and 35 inches or more in women. Abdominal obesity raises the risk of developing disorders, such as DIABETES; HYPERTENSION; and METABOLIC SYNDROME.
UMLS ID:: C0311277
MeSH ID:: D056128

Classification 1:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654.726.500.697

Classification 2:

Name:

Diagnosis
MeSH Tree Number(s):: E01.370.600.115.100.160.120.699.500.249

Classification 3:

Name:

Physiological Phenomena
MeSH Tree Number(s):: G07.100.100.160.120.699.500.249

Synonym(s)

Obesity, Abdominal

Abdominal obesity

Central obesity

Obesity;abdominal

abdominal obesity

Associated Drug(s)

	Name	Reference(s)	Data Source
1	1,2,3,4,6,7,8-heptachlorodibenzofuran	26752053	CTD
2	1,2,3,7,8-pentachlorodibenzo-p-dioxin	26752053	CTD
3	1,2,3,7,8-pentachlorodibenzofuran	26752053	CTD
4	2,3,4,7,8-pentachlorodibenzofuran	26752053	CTD
5	2,3,7,8-tetrachlorodibenzofuran	26752053	CTD
6	Letrozole	31295448	CTD
7	Polychlorinated Dibenzodioxins	26752053	CTD
8	Spironolactone	31295448	CTD
9	bis(4-hydroxyphenyl)sulfone	31528831	CTD
10	bisphenol A	21676388	CTD
11	bisphenol F	31528831	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Pediatric Obesity	42.4%
2	Underweight	20.8%
3	Body Height	16.3%
4	Birth Weight	15.9%
5	Body mass index	14.4%
6	Wasting Syndrome	13.3%
7	Fetal Weight	13%
8	Child Nutrition Disorders	12.2%
9	Hypervitaminosis A	12.2%
10	Infant Nutrition Disorders	12.2%
11	Malnutrition	12.2%
12	Prader-Willi Syndrome	12.2%
13	Apgar Score	11.4%
14	Auscultation	11.4%
15	Body Temperature	10.2%
16	Facies	9.2%
17	Disease susceptibility	8.1%
18	Electroencephalogram	7.9%
19	Metabolic Diseases	7.6%
20	Deficiency Diseases	7.2%
21	Starvation	7.2%
22	Refeeding Syndrome	7.2%
23	Autopsy	6.8%
24	angiogram	5.9%
25	Electrocardiogram	5.9%
26	Abnormal Involuntary Movement Scale	5.7%
27	HIV Wasting Syndrome	4.9%
28	Kwashiorkor	4.8%
29	Magnesium Deficiency	4.8%
30	Potassium Deficiency	4.8%
31	Protein Deficiency	4.8%
32	Avitaminosis	4.8%
33	Blood Pressure	4.6%
34	heart rate	4.6%
35	Respiratory rate	4.6%
36	Rickets	4.5%
37	Laryngoscopy	4.3%
38	Bronchoscopy	4.3%
39	Cystoscopy	4.3%
40	Glucose tolerance test	4.1%
41	Acid-Base Imbalance	4.1%
42	Calcium Metabolism Disorders	4.1%
43	Iron Metabolism Disorders	4.1%
44	Phosphorus Metabolism Disorders	4.1%
45	Water-Electrolyte Imbalance	4.1%
46	Lipid Metabolism Disorders	4.1%
47	Mitochondrial Diseases	4.1%
48	Glucose Metabolism Disorders	4.1%
49	Hyperhomocysteinemia	4%
50	Capillary Fragility	4%
51	Hypercalcemia	3.9%
52	Hypocalcemia	3.9%
53	Milk-Alkali Syndrome	3.9%
54	Colposcopy	3.8%
55	Hysteroscopy	3.8%
56	Biopsy	3.6%
57	Ascorbic Acid Deficiency	3.6%
58	Vitamin A Deficiency	3.6%
59	Vitamin D Deficiency	3.6%
60	Vitamin E Deficiency	3.6%
61	Marasmus	3.6%
62	Microscopy	3.4%
63	Osteomalacia	3.4%
64	Pleural Rub	3.3%
65	Rales	3.3%
66	Respiratory Sounds	3.3%
67	Rhonchi	3.3%
68	Stridor	3.3%
69	Wheezing	3.3%
70	Osteopenia	3.3%
71	Brain Diseases, Metabolic	3.3%
72	Lipodystrophy	3.2%
73	Pseudohypoparathyroidism	3.2%
74	Endoscopic Retrograde Cholangiopancreatography	3.1%
75	Folic Acid Deficiency	3%
76	Pellagra	3%
77	Thiamine Deficiency	3%
78	Vitamin B 12 Deficiency	3%
79	Vitamin B 6 Deficiency	3%
80	Pyridoxine Deficiency	3%
81	Valsalva Maneuver	2.9%
82	Oxidative Stress	2.8%
83	Brain Diseases, Metabolic, Inborn	2.8%
84	Leigh Disease	2.7%
85	Beriberi	2.7%
86	Familial Hypophosphatemic Rickets	2.6%
87	Wernicke Encephalopathy	2.6%
88	Vitamin K Deficiency	2.4%
89	Acidosis	2.4%
90	Alkalosis	2.4%
91	Amyloidosis	2.4%
92	Calcinosis	2.4%
93	Hyperglycemia	2.4%
94	Hyperinsulinism	2.4%
95	Hyperkalemia	2.4%
96	Hypernatremia	2.4%
97	Hypoglycemia	2.4%
98	Hypokalemia	2.4%
99	Hyponatremia	2.4%
100	Xanthomatosis	2.4%
101	Hypophosphatemia	2.4%
102	Metabolic acidosis	2.4%
103	Dyslipidemias	2.4%
104	Iron Overload	2.4%
105	Xanthoma	2.4%
106	Carbamoyl-Phosphate Synthase I Deficiency Disease	2.4%
107	Renal Osteodystrophy	2.4%
108	Renal rickets	2.4%
109	Lactose Intolerance	2.3%
110	Reflex, Abnormal	2.2%
111	Hyporeflexia	2.2%
112	Hyperreflexia	2.2%
113	Smith-Lemli-Opitz Syndrome	2.1%
114	Anemia, Pernicious	2.1%
115	Galactosemias	2.1%
116	Urea Cycle Disorders, Inborn	2.1%
117	Tyrosinemias	2.1%
118	Hypolipoproteinemias	2.1%
119	Hyperlipoproteinemia Type IV	2%
120	Hyperlipoproteinemia Type V	2%
121	Amniocentesis	2%
122	Mitochondrial Encephalomyopathies	2%
123	Diabetes Mellitus	2%
124	Glomerular Filtration Rate	2%
125	Scurvy	2%
126	Insulin Resistance	2%
127	Sweating	2%
128	Cardiac Output	2%
129	Laparoscopy	2%
130	Blood culture	2%
131	Dehydration	2%
132	Lipomatosis	2%
133	Water Intoxication	2%
134	Werner Syndrome	2%
135	Achlorhydria	1.9%
136	Amino Acid Metabolism, Inborn Errors	1.9%
137	Bloom Syndrome	1.9%
138	Carbohydrate Metabolism, Inborn Errors	1.9%
139	Metal Metabolism, Inborn Errors	1.9%
140	Osteoporosis	1.9%
141	Progeria	1.9%
142	Lysosomal Storage Diseases	1.9%
143	Bone Demineralization, Pathologic	1.9%
144	Cytochrome-c Oxidase Deficiency	1.9%
145	Peroxisomal Disorders	1.9%
146	Post-Traumatic Osteoporosis	1.9%
147	Celiac Disease	1.9%
148	Sprue, Tropical	1.9%
149	Steatorrhea	1.9%
150	Sprue	1.9%
151	Hyperphosphaturia	1.9%
152	Congenital Hyperinsulinism	1.9%
153	Diabetic Ketoacidosis	1.9%
154	Hyperlipidemia, Familial Combined	1.9%
155	Anion Gap	1.8%
156	Breast Feeding	1.8%
157	Homocystinuria	1.8%
158	Glycogen storage disease type II	1.7%
159	Hyperlipoproteinemia Type III	1.7%
160	Gaucher Disease	1.7%
161	Drug resistance	1.7%
162	Drug Tolerance	1.7%
163	Arthroscopy	1.7%
164	Mediastinoscopy	1.7%
165	Mitochondrial Myopathies	1.6%
166	Myelinolysis, Central Pontine	1.6%
167	Glycosuria	1.6%
168	Reye Syndrome	1.6%
169	Amyloid Neuropathies, Familial	1.6%
170	Hepatic Encephalopathy	1.6%
171	Renal tubular acidosis	1.6%
172	Acidosis, Lactic	1.6%
173	Calciphylaxis	1.6%
174	Hemosiderosis	1.6%
175	Ketosis	1.6%
176	Ketonuria	1.6%
177	Ketoacidosis	1.6%
178	Ketonemia	1.6%
179	Vascular calcification	1.6%
180	Hypoalphalipoproteinemias	1.6%
181	Adrenoleukodystrophy	1.5%
182	Zellweger Syndrome	1.5%
183	Menkes Kinky Hair Syndrome	1.5%
184	MELAS Syndrome	1.5%
185	Cytogenetic Analysis	1.5%
186	HIV-Associated Lipodystrophy Syndrome	1.4%
187	Porphyrias, Hepatic	1.4%
188	Neuronal Ceroid-Lipofuscinoses	1.4%
189	Tay-Sachs Disease	1.4%
190	Hepatolenticular Degeneration	1.4%
191	Niemann-Pick Disease, Type C	1.4%
192	Subacute Combined Degeneration	1.4%
193	Necrobiosis Lipoidica Diabeticorum	1.4%
194	Fanconi Anemia	1.4%
195	Nesidioblastosis	1.4%
196	Refsum Disease	1.4%
197	Fabry Disease	1.4%
198	Acidosis, Respiratory	1.3%
199	Adiposis Dolorosa	1.3%
200	Alkalosis, Respiratory	1.3%
201	Glycosuria, Renal	1.3%
202	Alkaptonuria	1.3%
203	Glycogen Storage Disease	1.3%
204	Hypophosphatasia	1.3%
205	Osteoporosis, Postmenopausal	1.3%
206	Propionic acidemia	1.3%
207	Dihydropyrimidine Dehydrogenase Deficiency	1.3%
208	Cystinosis	1.3%
209	Fasting	1.2%
210	Friedreich Ataxia	1.2%
211	Shivering	1.2%
212	Mucopolysaccharidosis III	1.2%
213	Hypercholesterolemia	1.2%
214	Hyperlipoproteinemias	1.2%
215	Hypertriglyceridemia	1.2%
216	Hunger	1.2%
217	Paracentesis	1.2%
218	Kearns-Sayre syndrome	1.1%
219	colonoscopy	1.1%
220	Proctoscopy	1.1%
221	Gestational Diabetes	1.1%
222	Latent Autoimmune Diabetes in Adults	1.1%
223	Kernicterus	1.1%
224	Diabetes Mellitus, Experimental	1.1%
225	Cockayne Syndrome	1.1%
226	treatment failure	1.1%
227	Nephrocalcinosis	1.1%
228	Tetany	1.1%
229	Cerebral Amyloid Angiopathy	1.1%
230	Total Lung Capacity	1%
231	Maximal Voluntary Ventilation	1%
232	Barium Enema	1%
233	Ataxia Telangiectasia	1%
234	Optic Atrophy, Hereditary, Leber	1%
235	Glycogen Storage Disease Type I	1%
236	Glycogen Storage Disease Type V	1%
237	Sjogren-Larsson Syndrome	0.9%
238	Familial Periodic Paralysis	0.9%
239	Primary amyloidosis	0.9%
240	Variegate Porphyria	0.9%
241	Acute intermittent porphyria	0.9%
242	Porphyria Cutanea Tarda	0.9%
243	Renal Aminoacidurias	0.9%
244	Fanconi Syndrome	0.9%
245	Pseudohypoaldosteronism	0.9%
246	Liddle Syndrome	0.9%
247	Xeroderma Pigmentosum	0.9%
248	Canavan Disease	0.9%
249	Alexander Disease	0.9%
250	Mucopolysaccharidosis II	0.9%
251	PROTHROMBIN TIME	0.9%
252	Tuberculin Test	0.8%
253	Clot retraction	0.8%
254	Gout	0.8%
255	Amyotrophic Lateral Sclerosis	0.8%
256	Bottle feeding	0.8%
257	Antley-Bixler Syndrome Phenotype	0.8%
258	venipuncture	0.7%
259	Diapedesis	0.7%
260	Tachyphylaxis	0.7%
261	Somatosensory Evoked Potentials	0.7%
262	CREST Syndrome	0.7%
263	Hypokalemic periodic paralysis	0.7%
264	Frontotemporal dementia	0.7%
265	Cystinuria	0.7%
266	Albinism	0.7%
267	Arthritis, Gouty	0.6%
268	Ichthyosis, X-Linked	0.5%
269	Peak expiratory flow rate	0.5%
270	Body Weight	0.5%
271	Body Weight Changes	0.4%
272	Ketogenic Diet	0.4%
273	Weight Gain	0.2%
274	Tidal Volume	0.2%

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