MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Deficiency Diseases

(UMLS:C0011156)

Definition:: A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed)
UMLS ID:: C0011156
MeSH ID:: D003677

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654.521.500

Synonym(s)

Deficiency Diseases

Deficiency diseases

deficiencies disease

deficiency disease

deficiency diseases

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Copper		12514262	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Starvation	46.7%
2	Refeeding Syndrome	46.7%
3	Kwashiorkor	34.4%
4	Child Nutrition Disorders	31%
5	Hypervitaminosis A	31%
6	Infant Nutrition Disorders	31%
7	Wasting Syndrome	27.9%
8	Metabolic Diseases	18.5%
9	Acid-Base Imbalance	10.3%
10	Calcium Metabolism Disorders	10.3%
11	Iron Metabolism Disorders	10.3%
12	Phosphorus Metabolism Disorders	10.3%
13	Water-Electrolyte Imbalance	10.3%
14	Lipid Metabolism Disorders	10.3%
15	Mitochondrial Diseases	10.3%
16	Glucose Metabolism Disorders	10.3%
17	Hypercalcemia	8.9%
18	Hypocalcemia	8.9%
19	Milk-Alkali Syndrome	8.9%
20	HIV Wasting Syndrome	8.8%
21	Obesity	7.8%
22	Obesity, Abdominal	7.2%
23	Osteopenia	7%
24	Brain Diseases, Metabolic	6.8%
25	Acidosis	6.7%
26	Alkalosis	6.7%
27	Amyloidosis	6.7%
28	Calcinosis	6.7%
29	Hyperglycemia	6.7%
30	Hyperinsulinism	6.7%
31	Hyperkalemia	6.7%
32	Hypernatremia	6.7%
33	Hypoglycemia	6.7%
34	Hypokalemia	6.7%
35	Hyponatremia	6.7%
36	Lipodystrophy	6.7%
37	Xanthomatosis	6.7%
38	Hypophosphatemia	6.7%
39	Metabolic acidosis	6.7%
40	Dyslipidemias	6.7%
41	Iron Overload	6.7%
42	Xanthoma	6.7%
43	Pseudohypoparathyroidism	6%
44	Pediatric Obesity	5.8%
45	Brain Diseases, Metabolic, Inborn	5.3%
46	Rickets	5.3%
47	Leigh Disease	5.1%
48	Prader-Willi Syndrome	4.9%
49	Acidosis, Lactic	4.9%
50	Calciphylaxis	4.9%
51	Hemosiderosis	4.9%
52	Ketosis	4.9%
53	Ketonuria	4.9%
54	Ketoacidosis	4.9%
55	Ketonemia	4.9%
56	Vascular calcification	4.9%
57	Hypolipoproteinemias	4.9%
58	Hyperlipoproteinemia Type IV	4.8%
59	Hyperlipoproteinemia Type V	4.8%
60	Diabetes Mellitus	4.8%
61	Carbamoyl-Phosphate Synthase I Deficiency Disease	4.6%
62	Lactose Intolerance	4.6%
63	Hyperhomocysteinemia	4.6%
64	Dehydration	4.5%
65	Lipomatosis	4.5%
66	Water Intoxication	4.5%
67	Werner Syndrome	4.5%
68	Diabetic Ketoacidosis	4.5%
69	Hyperlipidemia, Familial Combined	4.5%
70	Achlorhydria	4.4%
71	Amino Acid Metabolism, Inborn Errors	4.4%
72	Bloom Syndrome	4.4%
73	Carbohydrate Metabolism, Inborn Errors	4.4%
74	Metal Metabolism, Inborn Errors	4.4%
75	Osteoporosis	4.4%
76	Progeria	4.4%
77	Lysosomal Storage Diseases	4.4%
78	Bone Demineralization, Pathologic	4.4%
79	Cytochrome-c Oxidase Deficiency	4.4%
80	Peroxisomal Disorders	4.4%
81	Post-Traumatic Osteoporosis	4.4%
82	Celiac Disease	4.4%
83	Sprue, Tropical	4.4%
84	Steatorrhea	4.4%
85	Sprue	4.4%
86	Hyperlipoproteinemia Type III	4.2%
87	Smith-Lemli-Opitz Syndrome	4.2%
88	Galactosemias	4.2%
89	Urea Cycle Disorders, Inborn	4.2%
90	Tyrosinemias	4.2%
91	Hypercholesterolemia	4.1%
92	Hyperlipoproteinemias	4.1%
93	Hypertriglyceridemia	4.1%
94	Congenital Hyperinsulinism	4.1%
95	Hypoalphalipoproteinemias	4%
96	Osteomalacia	3.9%
97	Mitochondrial Encephalomyopathies	3.8%
98	Familial Hypophosphatemic Rickets	3.7%
99	Gaucher Disease	3.6%
100	Hyperphosphaturia	3.6%
101	Glycogen storage disease type II	3.5%
102	Homocystinuria	3.5%
103	Mitochondrial Myopathies	3.4%
104	Myelinolysis, Central Pontine	3.4%
105	Glycosuria	3.3%
106	Reye Syndrome	3.3%
107	Acidosis, Respiratory	3.3%
108	Adiposis Dolorosa	3.3%
109	Alkalosis, Respiratory	3.3%
110	Hepatic Encephalopathy	3.3%
111	Tay-Sachs Disease	3.3%
112	Nesidioblastosis	3.3%
113	Alkaptonuria	3.3%
114	Glycogen Storage Disease	3.3%
115	Hypophosphatasia	3.3%
116	Insulin Resistance	3.3%
117	Osteoporosis, Postmenopausal	3.3%
118	Propionic acidemia	3.3%
119	Dihydropyrimidine Dehydrogenase Deficiency	3.3%
120	Cystinosis	3.3%
121	Amyloid Neuropathies, Familial	3.3%
122	Renal tubular acidosis	3.2%
123	Niemann-Pick Disease, Type C	3.1%
124	Neuronal Ceroid-Lipofuscinoses	3%
125	Fabry Disease	2.8%
126	HIV-Associated Lipodystrophy Syndrome	2.8%
127	MELAS Syndrome	2.7%
128	Porphyrias, Hepatic	2.7%
129	Glycogen Storage Disease Type I	2.7%
130	Glycogen Storage Disease Type V	2.7%
131	Zellweger Syndrome	2.7%
132	Mucopolysaccharidosis III	2.7%
133	Adrenoleukodystrophy	2.7%
134	Necrobiosis Lipoidica Diabeticorum	2.6%
135	Menkes Kinky Hair Syndrome	2.6%
136	Fanconi Anemia	2.6%
137	Gestational Diabetes	2.6%
138	Latent Autoimmune Diabetes in Adults	2.6%
139	Diabetes Mellitus, Experimental	2.5%
140	Hepatolenticular Degeneration	2.5%
141	Nephrocalcinosis	2.5%
142	Tetany	2.5%
143	Renal Osteodystrophy	2.4%
144	Renal rickets	2.4%
145	Refsum Disease	2.4%
146	Glycosuria, Renal	2.4%
147	Cerebral Amyloid Angiopathy	2.4%
148	Wernicke Encephalopathy	2.2%
149	Friedreich Ataxia	2.2%
150	Familial Periodic Paralysis	2%
151	Primary amyloidosis	2%
152	Variegate Porphyria	2%
153	Acute intermittent porphyria	2%
154	Porphyria Cutanea Tarda	2%
155	Renal Aminoacidurias	1.9%
156	Fanconi Syndrome	1.9%
157	Pseudohypoaldosteronism	1.9%
158	Liddle Syndrome	1.9%
159	Kernicterus	1.9%
160	Kearns-Sayre syndrome	1.9%
161	Cockayne Syndrome	1.9%
162	Canavan Disease	1.8%
163	Alexander Disease	1.8%
164	Sjogren-Larsson Syndrome	1.8%
165	Mucopolysaccharidosis II	1.8%
166	Ataxia Telangiectasia	1.7%
167	Gout	1.7%
168	Amyotrophic Lateral Sclerosis	1.7%
169	Optic Atrophy, Hereditary, Leber	1.6%
170	Antley-Bixler Syndrome Phenotype	1.6%
171	Hypokalemic periodic paralysis	1.6%
172	Frontotemporal dementia	1.6%
173	Cystinuria	1.6%
174	Xeroderma Pigmentosum	1.5%
175	CREST Syndrome	1.4%
176	Arthritis, Gouty	1.4%
177	Albinism	1.2%
178	Ichthyosis, X-Linked	1%

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