MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Infant Nutrition Disorders

(UMLS:C0021280)

Definition:: Disorders caused by nutritional imbalance, either overnutrition or undernutrition, occurring in infants ages 1 month to 24 months.
UMLS ID:: C0021280
MeSH ID:: D007228

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654.422

Synonym(s)

Infant Nutrition Disorders

Nutrition disorders in infants

infant nutrition disorder

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Mebendazole		14747671	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Child Nutrition Disorders	42.9%
2	Hypervitaminosis A	42.9%
3	Malnutrition	42.9%
4	Wasting Syndrome	38.1%
5	Deficiency Diseases	31%
6	Starvation	31%
7	Refeeding Syndrome	31%
8	Kwashiorkor	25.4%
9	Magnesium Deficiency	25.4%
10	Potassium Deficiency	25.4%
11	Protein Deficiency	25.4%
12	Avitaminosis	25.4%
13	Metabolic Diseases	23.1%
14	Ascorbic Acid Deficiency	22.7%
15	Vitamin A Deficiency	22.7%
16	Vitamin D Deficiency	22.7%
17	Vitamin E Deficiency	22.7%
18	Marasmus	22.7%
19	Folic Acid Deficiency	21.3%
20	Pellagra	21.3%
21	Thiamine Deficiency	21.3%
22	Vitamin B 12 Deficiency	21.3%
23	Vitamin B 6 Deficiency	21.3%
24	Pyridoxine Deficiency	21.3%
25	Beriberi	20.7%
26	Rickets	16.5%
27	Hyperhomocysteinemia	15.7%
28	Osteomalacia	14.6%
29	Acid-Base Imbalance	14.3%
30	Calcium Metabolism Disorders	14.3%
31	Iron Metabolism Disorders	14.3%
32	Phosphorus Metabolism Disorders	14.3%
33	Water-Electrolyte Imbalance	14.3%
34	Lipid Metabolism Disorders	14.3%
35	Mitochondrial Diseases	14.3%
36	Glucose Metabolism Disorders	14.3%
37	Hypercalcemia	13.6%
38	Hypocalcemia	13.6%
39	Milk-Alkali Syndrome	13.6%
40	Anemia, Pernicious	13.5%
41	HIV Wasting Syndrome	13.3%
42	Obesity, Abdominal	12.2%
43	Obesity	11.8%
44	Vitamin K Deficiency	11.3%
45	Scurvy	10.6%
46	Acidosis	10.3%
47	Alkalosis	10.3%
48	Amyloidosis	10.3%
49	Calcinosis	10.3%
50	Hyperglycemia	10.3%
51	Hyperinsulinism	10.3%
52	Hyperkalemia	10.3%
53	Hypernatremia	10.3%
54	Hypoglycemia	10.3%
55	Hypokalemia	10.3%
56	Hyponatremia	10.3%
57	Xanthomatosis	10.3%
58	Hypophosphatemia	10.3%
59	Metabolic acidosis	10.3%
60	Dyslipidemias	10.3%
61	Iron Overload	10.3%
62	Xanthoma	10.3%
63	Lipodystrophy	10.2%
64	Wernicke Encephalopathy	10.2%
65	Pediatric Obesity	9.7%
66	Familial Hypophosphatemic Rickets	9.6%
67	Osteopenia	9.5%
68	Pseudohypoparathyroidism	9.4%
69	Brain Diseases, Metabolic	9.3%
70	Renal Osteodystrophy	9.1%
71	Renal rickets	9.1%
72	Hyperlipoproteinemia Type IV	8.8%
73	Hyperlipoproteinemia Type V	8.8%
74	Acidosis, Lactic	8.5%
75	Calciphylaxis	8.5%
76	Hemosiderosis	8.5%
77	Ketosis	8.5%
78	Ketonuria	8.5%
79	Ketoacidosis	8.5%
80	Ketonemia	8.5%
81	Vascular calcification	8.5%
82	Leigh Disease	8.4%
83	Prader-Willi Syndrome	8.3%
84	Hypolipoproteinemias	8.3%
85	Brain Diseases, Metabolic, Inborn	8.1%
86	Carbamoyl-Phosphate Synthase I Deficiency Disease	7.9%
87	Diabetic Ketoacidosis	7.9%
88	Hyperlipidemia, Familial Combined	7.8%
89	Hyperlipoproteinemia Type III	7.6%
90	Hypercholesterolemia	7.6%
91	Hyperlipoproteinemias	7.6%
92	Hypertriglyceridemia	7.6%
93	Hypoalphalipoproteinemias	7.3%
94	Diabetes Mellitus	7.3%
95	Lactose Intolerance	7.3%
96	Smith-Lemli-Opitz Syndrome	7%
97	Subacute Combined Degeneration	7%
98	Galactosemias	7%
99	Urea Cycle Disorders, Inborn	7%
100	Tyrosinemias	7%
101	Dehydration	7%
102	Lipomatosis	7%
103	Water Intoxication	7%
104	Werner Syndrome	7%
105	Gaucher Disease	6.9%
106	Congenital Hyperinsulinism	6.8%
107	Achlorhydria	6.8%
108	Amino Acid Metabolism, Inborn Errors	6.8%
109	Bloom Syndrome	6.8%
110	Carbohydrate Metabolism, Inborn Errors	6.8%
111	Metal Metabolism, Inborn Errors	6.8%
112	Osteoporosis	6.8%
113	Progeria	6.8%
114	Lysosomal Storage Diseases	6.8%
115	Bone Demineralization, Pathologic	6.8%
116	Cytochrome-c Oxidase Deficiency	6.8%
117	Peroxisomal Disorders	6.8%
118	Post-Traumatic Osteoporosis	6.8%
119	Celiac Disease	6.7%
120	Sprue, Tropical	6.7%
121	Steatorrhea	6.7%
122	Sprue	6.7%
123	Tay-Sachs Disease	6.5%
124	Glycogen storage disease type II	6.4%
125	Hyperphosphaturia	6.1%
126	Mitochondrial Encephalomyopathies	6.1%
127	Niemann-Pick Disease, Type C	6%
128	Nesidioblastosis	6%
129	Homocystinuria	6%
130	Amyloid Neuropathies, Familial	5.7%
131	Acidosis, Respiratory	5.6%
132	Adiposis Dolorosa	5.6%
133	Alkalosis, Respiratory	5.6%
134	Alkaptonuria	5.6%
135	Glycogen Storage Disease	5.6%
136	Hypophosphatasia	5.6%
137	Insulin Resistance	5.6%
138	Osteoporosis, Postmenopausal	5.6%
139	Propionic acidemia	5.6%
140	Dihydropyrimidine Dehydrogenase Deficiency	5.6%
141	Cystinosis	5.6%
142	Renal tubular acidosis	5.4%
143	Fabry Disease	5.3%
144	Neuronal Ceroid-Lipofuscinoses	5.2%
145	Mitochondrial Myopathies	5.2%
146	Myelinolysis, Central Pontine	5.1%
147	Glycosuria	5%
148	Reye Syndrome	5%
149	Hepatic Encephalopathy	5%
150	Glycogen Storage Disease Type I	4.9%
151	Glycogen Storage Disease Type V	4.9%
152	Mucopolysaccharidosis III	4.9%
153	MELAS Syndrome	4.7%
154	HIV-Associated Lipodystrophy Syndrome	4.7%
155	Adrenoleukodystrophy	4.6%
156	Zellweger Syndrome	4.5%
157	Menkes Kinky Hair Syndrome	4.4%
158	Gestational Diabetes	4.3%
159	Latent Autoimmune Diabetes in Adults	4.3%
160	Diabetes Mellitus, Experimental	4.3%
161	Nephrocalcinosis	4.2%
162	Tetany	4.2%
163	Hepatolenticular Degeneration	4.1%
164	Porphyrias, Hepatic	4.1%
165	Cerebral Amyloid Angiopathy	4.1%
166	Glycosuria, Renal	4.1%
167	Refsum Disease	4.1%
168	Necrobiosis Lipoidica Diabeticorum	4%
169	Fanconi Anemia	4%
170	Familial Periodic Paralysis	3.4%
171	Primary amyloidosis	3.4%
172	Variegate Porphyria	3.3%
173	Acute intermittent porphyria	3.3%
174	Porphyria Cutanea Tarda	3.3%
175	Friedreich Ataxia	3.3%
176	Renal Aminoacidurias	3.3%
177	Fanconi Syndrome	3.3%
178	Pseudohypoaldosteronism	3.3%
179	Liddle Syndrome	3.3%
180	Canavan Disease	3.3%
181	Alexander Disease	3.3%
182	Mucopolysaccharidosis II	3.2%
183	Sjogren-Larsson Syndrome	3.1%
184	Kearns-Sayre syndrome	3.1%
185	Hypokalemic periodic paralysis	3%
186	Frontotemporal dementia	2.9%
187	Cystinuria	2.9%
188	Kernicterus	2.9%
189	Cockayne Syndrome	2.9%
190	Gout	2.8%
191	Amyotrophic Lateral Sclerosis	2.8%
192	Antley-Bixler Syndrome Phenotype	2.7%
193	Ataxia Telangiectasia	2.5%
194	Optic Atrophy, Hereditary, Leber	2.5%
195	Arthritis, Gouty	2.5%
196	CREST Syndrome	2.3%
197	Xeroderma Pigmentosum	2.3%
198	Albinism	2.1%
199	Ichthyosis, X-Linked	1.7%

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