MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Wasting Syndrome

(UMLS:C0043046)

Definition:: A condition of involuntary weight loss of greater then 10% of baseline body weight. It is characterized by atrophy of muscles and depletion of lean body mass. Wasting is a sign of MALNUTRITION as a result of inadequate dietary intake, malabsorption, or hypermetabolism.
UMLS ID:: C0043046
MeSH ID:: D019282

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.915|C18.654.940

Synonym(s)

Wasting Syndrome

Malnutrition/starvation/cachexia

WASTING SYNDROME

Wasting disease

Wasting disease, NOS

Wasting syndrome

disease (or disorder); wasting

disease; wasting

syndrome; wasting

10.

wasting disease

11.

wasting diseases

12.

wasting syndrome

13.

wasting; disease

14.

wasting; syndrome

Associated Drug(s)

	Name	Reference(s)	Data Source
1	3,4,5,3',4'-pentachlorobiphenyl	28163111	CTD
2	Choline	28163111	CTD
3	Methionine	28163111	CTD
4	Polychlorinated Dibenzodioxins	View details 1400292 15886252 19420757 20876576 21215274 25529477 25975270 28774668 29873790	CTD
5	Resveratrol	19420757	CTD
6	Stavudine	12008857	CTD
7	Zidovudine	9268244	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Hypercalcemia	41.4%
2	Hypocalcemia	41.4%
3	Milk-Alkali Syndrome	41.4%
4	Acid-Base Imbalance	38.1%
5	Calcium Metabolism Disorders	38.1%
6	Child Nutrition Disorders	38.1%
7	Iron Metabolism Disorders	38.1%
8	Hypervitaminosis A	38.1%
9	Infant Nutrition Disorders	38.1%
10	Phosphorus Metabolism Disorders	38.1%
11	Water-Electrolyte Imbalance	38.1%
12	Lipid Metabolism Disorders	38.1%
13	Malnutrition	38.1%
14	Mitochondrial Diseases	38.1%
15	Glucose Metabolism Disorders	38.1%
16	Rickets	36.6%
17	Hyperhomocysteinemia	33.9%
18	Lipodystrophy	32.9%
19	Pseudohypoparathyroidism	32.7%
20	Osteomalacia	31.2%
21	Leigh Disease	30%
22	Hyperlipoproteinemia Type IV	29.8%
23	Hyperlipoproteinemia Type V	29.8%
24	Familial Hypophosphatemic Rickets	28.6%
25	Osteopenia	28.6%
26	Carbamoyl-Phosphate Synthase I Deficiency Disease	28.3%
27	Brain Diseases, Metabolic	28.1%
28	Acidosis	27.9%
29	Alkalosis	27.9%
30	Amyloidosis	27.9%
31	Calcinosis	27.9%
32	Deficiency Diseases	27.9%
33	Hyperglycemia	27.9%
34	Hyperinsulinism	27.9%
35	Hyperkalemia	27.9%
36	Hypernatremia	27.9%
37	Hypoglycemia	27.9%
38	Hypokalemia	27.9%
39	Hyponatremia	27.9%
40	Starvation	27.9%
41	Xanthomatosis	27.9%
42	Hypophosphatemia	27.9%
43	Metabolic acidosis	27.9%
44	Dyslipidemias	27.9%
45	Iron Overload	27.9%
46	Xanthoma	27.9%
47	Refeeding Syndrome	27.9%
48	Brain Diseases, Metabolic, Inborn	27.1%
49	Hypolipoproteinemias	26.8%
50	Diabetic Ketoacidosis	25.6%
51	Hyperlipidemia, Familial Combined	25.4%
52	Gaucher Disease	25.2%
53	Smith-Lemli-Opitz Syndrome	24.9%
54	Galactosemias	24.7%
55	Urea Cycle Disorders, Inborn	24.7%
56	Tyrosinemias	24.7%
57	Hyperlipoproteinemia Type III	24.7%
58	Lactose Intolerance	24.6%
59	Hypoalphalipoproteinemias	23.9%
60	Tay-Sachs Disease	23.7%
61	Glycogen storage disease type II	23.4%
62	Acidosis, Lactic	23%
63	Calciphylaxis	23%
64	Hemosiderosis	23%
65	Ketosis	23%
66	Kwashiorkor	23%
67	Magnesium Deficiency	23%
68	Potassium Deficiency	23%
69	Protein Deficiency	23%
70	Ketonuria	23%
71	Ketoacidosis	23%
72	Ketonemia	23%
73	Vascular calcification	23%
74	Avitaminosis	23%
75	Congenital Hyperinsulinism	23%
76	Niemann-Pick Disease, Type C	22.2%
77	Hyperphosphaturia	21.9%
78	Diabetes Mellitus	21.8%
79	Homocystinuria	21.4%
80	Dehydration	21.1%
81	Lipomatosis	21.1%
82	Water Intoxication	21.1%
83	Werner Syndrome	21.1%
84	Mitochondrial Encephalomyopathies	21.1%
85	Renal Osteodystrophy	20.7%
86	Renal rickets	20.7%
87	Achlorhydria	20.7%
88	Amino Acid Metabolism, Inborn Errors	20.7%
89	Bloom Syndrome	20.7%
90	Carbohydrate Metabolism, Inborn Errors	20.7%
91	Metal Metabolism, Inborn Errors	20.7%
92	Osteoporosis	20.7%
93	Progeria	20.7%
94	Lysosomal Storage Diseases	20.7%
95	Bone Demineralization, Pathologic	20.7%
96	Cytochrome-c Oxidase Deficiency	20.7%
97	Peroxisomal Disorders	20.7%
98	Post-Traumatic Osteoporosis	20.7%
99	Amyloid Neuropathies, Familial	20.6%
100	Ascorbic Acid Deficiency	20.6%
101	Hypercholesterolemia	20.6%
102	Hyperlipoproteinemias	20.6%
103	Hypertriglyceridemia	20.6%
104	Vitamin A Deficiency	20.6%
105	Vitamin D Deficiency	20.6%
106	Vitamin E Deficiency	20.6%
107	Marasmus	20.6%
108	Celiac Disease	20.5%
109	Sprue, Tropical	20.5%
110	Steatorrhea	20.5%
111	Sprue	20.5%
112	Nesidioblastosis	20.1%
113	Fabry Disease	19.8%
114	Wernicke Encephalopathy	19.4%
115	Folic Acid Deficiency	19.4%
116	Pellagra	19.4%
117	Thiamine Deficiency	19.4%
118	Vitamin B 12 Deficiency	19.4%
119	Vitamin B 6 Deficiency	19.4%
120	Pyridoxine Deficiency	19.4%
121	Renal tubular acidosis	18.9%
122	Beriberi	18.8%
123	Neuronal Ceroid-Lipofuscinoses	18.1%
124	Adrenoleukodystrophy	17.3%
125	MELAS Syndrome	17.2%
126	Acidosis, Respiratory	17.1%
127	Adiposis Dolorosa	17.1%
128	Alkalosis, Respiratory	17.1%
129	Alkaptonuria	16.9%
130	Glycogen Storage Disease	16.9%
131	Hypophosphatasia	16.9%
132	Insulin Resistance	16.9%
133	Osteoporosis, Postmenopausal	16.9%
134	Propionic acidemia	16.9%
135	Dihydropyrimidine Dehydrogenase Deficiency	16.9%
136	Cystinosis	16.9%
137	Mucopolysaccharidosis III	16.9%
138	Mitochondrial Myopathies	16.7%
139	Zellweger Syndrome	16.6%
140	HIV-Associated Lipodystrophy Syndrome	16.6%
141	Myelinolysis, Central Pontine	16.6%
142	Menkes Kinky Hair Syndrome	16.4%
143	Glycosuria	16.3%
144	Reye Syndrome	16.3%
145	Hepatic Encephalopathy	16.2%
146	Hepatolenticular Degeneration	15.3%
147	Glycogen Storage Disease Type I	15.1%
148	Glycogen Storage Disease Type V	15.1%
149	Refsum Disease	15.1%
150	Metabolic Diseases	15%
151	Nutrition Disorders	15%
152	Glycosuria, Renal	14.6%
153	Wasting Syndrome	14.3%
154	Gestational Diabetes	14%
155	Latent Autoimmune Diabetes in Adults	14%
156	Anemia, Pernicious	13.8%
157	Diabetes Mellitus, Experimental	13.8%
158	Porphyrias, Hepatic	13.8%
159	Necrobiosis Lipoidica Diabeticorum	13.6%
160	Nephrocalcinosis	13.5%
161	Tetany	13.5%
162	Fanconi Anemia	13.4%
163	Cerebral Amyloid Angiopathy	13.3%
164	Obesity	13.3%
165	Obesity, Abdominal	13.3%
166	Vitamin K Deficiency	12.2%
167	Canavan Disease	11.9%
168	Alexander Disease	11.9%
169	Mucopolysaccharidosis II	11.7%
170	Kearns-Sayre syndrome	11.4%
171	Scurvy	11.4%
172	Sjogren-Larsson Syndrome	11.4%
173	Friedreich Ataxia	11.4%
174	Familial Periodic Paralysis	11.4%
175	Primary amyloidosis	11.3%
176	Variegate Porphyria	11.2%
177	Acute intermittent porphyria	11.2%
178	Porphyria Cutanea Tarda	11.2%
179	Renal Aminoacidurias	11.1%
180	Fanconi Syndrome	11.1%
181	Pseudohypoaldosteronism	11.1%
182	Liddle Syndrome	11.1%
183	Pediatric Obesity	11%
184	Kernicterus	10.2%
185	Cockayne Syndrome	10.1%
186	Hypokalemic periodic paralysis	10%
187	Frontotemporal dementia	9.9%
188	Cystinuria	9.9%
189	Gout	9.7%
190	Amyotrophic Lateral Sclerosis	9.7%
191	Prader-Willi Syndrome	9.6%
192	Antley-Bixler Syndrome Phenotype	9.5%
193	Ataxia Telangiectasia	9.1%
194	Optic Atrophy, Hereditary, Leber	8.8%
195	Arthritis, Gouty	8.5%
196	CREST Syndrome	8.3%
197	Xeroderma Pigmentosum	8.2%
198	Subacute Combined Degeneration	8.1%
199	Albinism	7.5%
200	Ichthyosis, X-Linked	6%
201	HIV Wasting Syndrome	5.8%

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