MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Nutrition Disorders

(UMLS:C3714509)

Definition:: Disorders caused by nutritional imbalance, either overnutrition or undernutrition.
UMLS ID:: C3714509
MeSH ID:: D009748

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654

Synonym(s)

Nutrition Disorders

Disorder of nutrition

Disorder;nutritional

Nutrition disorders

Nutritional Disorder

Nutritional disease

Nutritional disease, NOS

Nutritional disorder

Nutritional disorder, NOS

10.

Problem;nutritional

11.

disease nutrition

12.

disease nutritional

13.

diseases nutrition

14.

diseases nutritional

15.

disorder nutrition

16.

disorder; nutritional

17.

disorders nutrition

18.

nutrition disease

19.

nutrition diseases

20.

nutrition disorder

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Vitamin D		9574950	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Metabolic Diseases	33.3%
2	Hypercalcemia	23.8%
3	Hypocalcemia	23.8%
4	Milk-Alkali Syndrome	23.8%
5	Acid-Base Imbalance	23.1%
6	Calcium Metabolism Disorders	23.1%
7	Iron Metabolism Disorders	23.1%
8	Phosphorus Metabolism Disorders	23.1%
9	Water-Electrolyte Imbalance	23.1%
10	Lipid Metabolism Disorders	23.1%
11	Mitochondrial Diseases	23.1%
12	Glucose Metabolism Disorders	23.1%
13	Acidosis	18.5%
14	Alkalosis	18.5%
15	Amyloidosis	18.5%
16	Calcinosis	18.5%
17	Hyperglycemia	18.5%
18	Hyperinsulinism	18.5%
19	Hyperkalemia	18.5%
20	Hypernatremia	18.5%
21	Hypoglycemia	18.5%
22	Hypokalemia	18.5%
23	Hyponatremia	18.5%
24	Xanthomatosis	18.5%
25	Hypophosphatemia	18.5%
26	Metabolic acidosis	18.5%
27	Dyslipidemias	18.5%
28	Iron Overload	18.5%
29	Xanthoma	18.5%
30	Lipodystrophy	17.5%
31	Hyperlipoproteinemia Type IV	17.1%
32	Hyperlipoproteinemia Type V	17.1%
33	Pseudohypoparathyroidism	16.5%
34	Acidosis, Lactic	16.4%
35	Calciphylaxis	16.4%
36	Hemosiderosis	16.4%
37	Ketosis	16.4%
38	Ketonuria	16.4%
39	Ketoacidosis	16.4%
40	Ketonemia	16.4%
41	Vascular calcification	16.4%
42	Hypolipoproteinemias	15.4%
43	Hypercholesterolemia	15.3%
44	Hyperlipoproteinemias	15.3%
45	Hypertriglyceridemia	15.3%
46	Leigh Disease	15.1%
47	Diabetic Ketoacidosis	15%
48	Osteopenia	15%
49	Wasting Syndrome	15%
50	Hyperlipidemia, Familial Combined	14.9%
51	Hyperlipoproteinemia Type III	14.6%
52	Brain Diseases, Metabolic	14.6%
53	Carbamoyl-Phosphate Synthase I Deficiency Disease	14.6%
54	Hypoalphalipoproteinemias	14.3%
55	Brain Diseases, Metabolic, Inborn	13.8%
56	Rickets	13.7%
57	Gaucher Disease	13.4%
58	Tay-Sachs Disease	13%
59	Lactose Intolerance	12.9%
60	Smith-Lemli-Opitz Syndrome	12.9%
61	Hyperhomocysteinemia	12.9%
62	Galactosemias	12.8%
63	Urea Cycle Disorders, Inborn	12.8%
64	Tyrosinemias	12.8%
65	Diabetes Mellitus	12.8%
66	Congenital Hyperinsulinism	12.7%
67	Familial Hypophosphatemic Rickets	12.7%
68	Glycogen storage disease type II	12.3%
69	Dehydration	12.2%
70	Lipomatosis	12.2%
71	Water Intoxication	12.2%
72	Werner Syndrome	12.2%
73	Osteomalacia	12.1%
74	Achlorhydria	11.9%
75	Amino Acid Metabolism, Inborn Errors	11.9%
76	Bloom Syndrome	11.9%
77	Carbohydrate Metabolism, Inborn Errors	11.9%
78	Metal Metabolism, Inborn Errors	11.9%
79	Osteoporosis	11.9%
80	Progeria	11.9%
81	Lysosomal Storage Diseases	11.9%
82	Bone Demineralization, Pathologic	11.9%
83	Cytochrome-c Oxidase Deficiency	11.9%
84	Peroxisomal Disorders	11.9%
85	Post-Traumatic Osteoporosis	11.9%
86	Niemann-Pick Disease, Type C	11.9%
87	Celiac Disease	11.8%
88	Sprue, Tropical	11.8%
89	Steatorrhea	11.8%
90	Sprue	11.8%
91	Nesidioblastosis	11.6%
92	Hyperphosphaturia	11.2%
93	Homocystinuria	11.1%
94	Amyloid Neuropathies, Familial	10.8%
95	Mitochondrial Encephalomyopathies	10.7%
96	Acidosis, Respiratory	10.6%
97	Adiposis Dolorosa	10.6%
98	Alkalosis, Respiratory	10.6%
99	Alkaptonuria	10.5%
100	Glycogen Storage Disease	10.5%
101	Hypophosphatasia	10.5%
102	Insulin Resistance	10.5%
103	Osteoporosis, Postmenopausal	10.5%
104	Propionic acidemia	10.5%
105	Dihydropyrimidine Dehydrogenase Deficiency	10.5%
106	Cystinosis	10.5%
107	Fabry Disease	10.3%
108	Renal tubular acidosis	10%
109	Neuronal Ceroid-Lipofuscinoses	9.8%
110	Glycogen Storage Disease Type I	9.8%
111	Glycogen Storage Disease Type V	9.8%
112	Mucopolysaccharidosis III	9.4%
113	Mitochondrial Myopathies	8.9%
114	Myelinolysis, Central Pontine	8.8%
115	Glycosuria	8.7%
116	Reye Syndrome	8.7%
117	MELAS Syndrome	8.7%
118	Hepatic Encephalopathy	8.6%
119	HIV-Associated Lipodystrophy Syndrome	8.6%
120	Adrenoleukodystrophy	8.4%
121	Zellweger Syndrome	8.2%
122	Gestational Diabetes	8.1%
123	Latent Autoimmune Diabetes in Adults	8.1%
124	Menkes Kinky Hair Syndrome	8.1%
125	Diabetes Mellitus, Experimental	8%
126	Nephrocalcinosis	7.8%
127	Tetany	7.8%
128	Cerebral Amyloid Angiopathy	7.6%
129	Hepatolenticular Degeneration	7.5%
130	Renal Osteodystrophy	7.5%
131	Renal rickets	7.5%
132	Glycosuria, Renal	7.4%
133	Refsum Disease	7.4%
134	Porphyrias, Hepatic	7%
135	Necrobiosis Lipoidica Diabeticorum	6.9%
136	Fanconi Anemia	6.8%
137	Canavan Disease	6.3%
138	Alexander Disease	6.3%
139	Familial Periodic Paralysis	6.2%
140	Primary amyloidosis	6.2%
141	Mucopolysaccharidosis II	6.2%
142	Variegate Porphyria	6.1%
143	Acute intermittent porphyria	6.1%
144	Porphyria Cutanea Tarda	6.1%
145	Renal Aminoacidurias	6.1%
146	Fanconi Syndrome	6.1%
147	Pseudohypoaldosteronism	6.1%
148	Liddle Syndrome	6.1%
149	Sjogren-Larsson Syndrome	5.8%
150	Hypokalemic periodic paralysis	5.7%
151	Frontotemporal dementia	5.7%
152	HIV Wasting Syndrome	5.7%
153	Cystinuria	5.7%
154	Wernicke Encephalopathy	5.7%
155	Friedreich Ataxia	5.6%
156	Kearns-Sayre syndrome	5.5%
157	Gout	5.2%
158	Amyotrophic Lateral Sclerosis	5.1%
159	Antley-Bixler Syndrome Phenotype	5%
160	Kernicterus	4.9%
161	Cockayne Syndrome	4.9%
162	Arthritis, Gouty	4.7%
163	Ataxia Telangiectasia	4.3%
164	CREST Syndrome	4.3%
165	Optic Atrophy, Hereditary, Leber	4.2%
166	Albinism	3.8%
167	Xeroderma Pigmentosum	3.8%
168	Ichthyosis, X-Linked	3%

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