MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Infant, Premature, Diseases

(UMLS:C0021295)

Definition:: Diseases that occur in PREMATURE INFANTS.
UMLS ID:: C0021295
MeSH ID:: D007235

Classification:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.614.521

Synonym(s)

Infant, Premature, Diseases

Premature infants--Diseases

disease infants premature

disease of premature infants

infant premature disease

premature infant diseases

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Acetazolamide	1622512	CTD
2	Aminophylline	7795341	CTD
3	Beclomethasone	11015126	CTD
4	Caffeine	11753270 19052555	CTD
5	Cocaine	11425091	CTD
6	Cytarabine	7529655	CTD
7	Daunorubicin	7529655	CTD
8	Dexamethasone	1537356 10380089	CTD
9	Diazepam	4807250	CTD
10	Digoxin	6880719	CTD
11	Doxapram	View details 9672531 11743509 11753270 16303710	CTD
12	Enalapril	8645963	CTD
13	Etoposide	7529655	CTD
14	Furosemide	View details 1622512 1815176 2264472 3275932 3279919 7110808 15351602 19460127	CTD
15	Hexachlorophene	958085	CTD
16	Ibuprofen	10974130 16133044	CTD
17	Indomethacin	View details 2766920 3050004 6377215 7019841 7108667 10516392 10974130 12970633 15046280 16133044	CTD
18	Isotretinoin	6591112	CTD
19	Lisinopril	8247923	CTD
20	Naproxen	533297	CTD
21	Phenobarbital	4096759	CTD
22	Theophylline	View details 22592 660340 7398750 11605782	CTD
23	Thiopental	19583708	CTD
24	caffeine citrate	6810291 7795341	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Abdominal Cramps	42.9%
2	Amniotic Band Syndrome	42.9%
3	Asphyxia Neonatorum	42.9%
4	Infantile Colic	42.9%
5	Anemia, Neonatal	27.9%
6	Persistent Fetal Circulation Syndrome	27.9%
7	Umbilical hernia	27.4%
8	Deformity	23.1%
9	Genetic Diseases, Inborn	23.1%
10	Cystic Fibrosis	22.9%
11	Neonatal Abstinence Syndrome	21.4%
12	Paralysis, Obstetric	20.9%
13	Xeroderma	20.5%
14	Mobius Syndrome	20.5%
15	Congenital nystagmus	20.5%
16	Toxoplasmosis, Congenital	20.3%
17	Syphilis, Congenital	20.2%
18	Meconium Aspiration Syndrome	18.6%
19	Congenital Hyperinsulinism	16.4%
20	Beckwith-Wiedemann Syndrome	15.3%
21	Wolf-Hirschhorn Syndrome	15.3%
22	Fetal Diseases	15%
23	Abnormalities, Drug-Induced	14.3%
24	Situs Inversus	14.3%
25	Ichthyosis, X-Linked	13.2%
26	Smith-Magenis syndrome	12.3%
27	Aicardi's syndrome	12.2%
28	Cri-du-Chat Syndrome	12.1%
29	Down Syndrome	12.1%
30	Trisomy 21	12.1%
31	CHARGE Syndrome	12.1%
32	Nesidioblastosis	11.9%
33	Holoprosencephaly	11.7%
34	Hyperkeratosis, Epidermolytic	11.4%
35	Ophthalmia Neonatorum	11.3%
36	Sjogren-Larsson Syndrome	11%
37	Fragile X Syndrome	10.9%
38	Familial Mediterranean Fever	10.3%
39	Prune Belly Syndrome	10.3%
40	Twins, Conjoined	10.3%
41	Waardenburg Syndrome	10.3%
42	Ectodermal Dysplasia	10.1%
43	Aplasia Cutis Congenita	10.1%
44	Eye Abnormalities	10%
45	Neoplastic Syndromes, Hereditary	10%
46	Prader-Willi Syndrome	10%
47	Cardiovascular Abnormalities	10%
48	Nail-Patella Syndrome	9.7%
49	Rubinstein-Taybi Syndrome	9.5%
50	Skin Abnormalities	9.5%
51	Lymphatic Abnormalities	9.5%
52	Congenital Microtia	9.5%
53	Multiple Epiphyseal Dysplasia	9.3%
54	Osteochondrodysplasias	9.3%
55	Pelger-Huet Anomaly	9.3%
56	Werner Syndrome	9.3%
57	Myasthenic Syndromes, Congenital	9.3%
58	Anencephaly	9.2%
59	Congenital diaphragmatic hernia	9.2%
60	Kernicterus	8.7%
61	Cockayne Syndrome	8.6%
62	Alstrom Syndrome	8.5%
63	Kartagener Syndrome	8.5%
64	Rett Syndrome	8.2%
65	Marfan Syndrome	8.1%
66	Primary Ciliary Dyskinesia	8%
67	Anemia, Sickle Cell	8%
68	Thalassemia	8%
69	Muscular Dystrophy, Duchenne	8%
70	Polycystic Kidney Diseases	8%
71	Williams Syndrome	8%
72	Smith-Lemli-Opitz Syndrome	7.5%
73	Maxillofacial Abnormalities	7.5%
74	Dural Arteriovenous Fistula	7.5%
75	Classical Lissencephalies and Subcortical Band Heterotopias	7.4%
76	Urogenital Abnormalities	7.4%
77	Dextrocardia	7.4%
78	Dwarfism	7.3%
79	Albinism	7.1%
80	Anophthalmos	7%
81	Anus, Imperforate	7%
82	Hydranencephaly	7%
83	Microphthalmos	7%
84	Neural Tube Defects	7%
85	Retinal Dysplasia	7%
86	Tethered Cord Syndrome	7%
87	Iniencephaly	7%
88	Craniorachischisis	7%
89	Limb Deformities, Congenital	7%
90	Exencephaly	7%
91	Septo-Optic Dysplasia	7%
92	Craniofacial Abnormalities	7%
93	Cortical Dysplasia	7%
94	Malformations of Cortical Development	7%
95	Anorectal Malformations	7%
96	Aniridia	6.9%
97	Fetal Growth Retardation	6.9%
98	Muscular Dystrophy	6.8%
99	Osteogenesis Imperfecta	6.8%
100	Fetal Hypoxia	6.8%
101	Fetal Alcohol Spectrum Disorders	6.8%
102	Mucopolysaccharidosis II	6.8%
103	Amino Acid Metabolism, Inborn Errors	6.8%
104	Bloom Syndrome	6.8%
105	Carbohydrate Metabolism, Inborn Errors	6.8%
106	Metal Metabolism, Inborn Errors	6.8%
107	Progeria	6.8%
108	Lysosomal Storage Diseases	6.8%
109	Cytochrome-c Oxidase Deficiency	6.8%
110	Peroxisomal Disorders	6.8%
111	Epidermolysis Bullosa	6.7%
112	Sickle Cell Trait	6.5%
113	Polycystic Kidney, Autosomal Dominant	6.5%
114	Microcephaly	6.3%
115	Macrocephaly	6.3%
116	Kallmann Syndrome	5.9%
117	Menkes Kinky Hair Syndrome	5.9%
118	Porencephaly	5.9%
119	Neuronal Ceroid-Lipofuscinoses	5.8%
120	Wiskott-Aldrich Syndrome	5.7%
121	Tuberous Sclerosis	5.6%
122	Amelia	5.6%
123	Arachnodactyly	5.6%
124	Ectopia Cordis	5.6%
125	Ectromelia	5.6%
126	Hemimelia	5.6%
127	Meningomyelocele	5.6%
128	Phocomelia	5.6%
129	Sirenomelia	5.6%
130	Spina Bifida	5.6%
131	Polydactyly	5.6%
132	Brachydactyly	5.6%
133	Plagiocephaly	5.6%
134	Lower Extremity Deformities, Congenital	5.6%
135	Upper Extremity Deformities, Congenital	5.6%
136	Single umbilical artery	5.6%
137	Alkaptonuria	5.6%
138	Glycogen Storage Disease	5.6%
139	Hypophosphatasia	5.6%
140	Propionic acidemia	5.6%
141	Autoimmune Lymphoproliferative Syndrome	5.6%
142	Dihydropyrimidine Dehydrogenase Deficiency	5.6%
143	Cystinosis	5.6%
144	Craniosynostosis	5.5%
145	Syndactyly	5.5%
146	Brachycephaly	5.5%
147	Klinefelter Syndrome	5.5%
148	Charcot-Marie-Tooth Disease	5.5%
149	Antley-Bixler Syndrome Phenotype	5.5%
150	Chorioamnionitis	5.4%
151	Refsum Disease	5.4%
152	Scimitar Syndrome	5.4%
153	Angioedemas, Hereditary	5.4%
154	Turner Syndrome	5.3%
155	Acrocephalosyndactylia	5.3%
156	Blepharophimosis	5.3%
157	Laryngostenosis	5.3%
158	Mouth Abnormalities	5.3%
159	Cutis Laxa	5.2%
160	Esophageal Atresia	5.2%
161	Intestinal Atresia	5.2%
162	Horseshoe Kidney	5.2%
163	Pectus excavatum	5.2%
164	Klippel-Feil Syndrome	5.1%
165	Retinitis Pigmentosa	5.1%
166	Gastroschisis	5.1%
167	Synostosis	5.1%
168	Pigmentary retinopathy	5.1%
169	Acrodermatitis	5.1%
170	Lymphangiectasis, Intestinal	5.1%
171	Porokeratosis	5.1%
172	Gianotti-Crosti Syndrome	5.1%
173	Keratoderma, Palmoplantar	5.1%
174	Pseudoxanthoma Elasticum	5.1%
175	Chronic granulomatous disease	5%
176	Welander Distal Myopathy	5%
177	Dermal Sinus	5%
178	Spina Bifida Cystica	5%
179	Spina Bifida Occulta	5%
180	Lissencephaly	5%
181	Polymicrogyria	5%
182	Pachygyria	5%
183	Schizencephaly	5%
184	Periventricular Nodular Heterotopia	5%
185	Myotonic Dystrophy	5%
186	Glycogen Storage Disease Type I	4.9%
187	Glycogen Storage Disease Type V	4.9%
188	Poland Syndrome	4.9%
189	Mucopolysaccharidosis III	4.9%
190	Glycogen storage disease type II	4.8%
191	Noonan Syndrome	4.8%
192	Zellweger Syndrome	4.8%
193	Acute Chest Syndrome	4.8%
194	Galactosemias	4.7%
195	Urea Cycle Disorders, Inborn	4.7%
196	Tyrosinemias	4.7%
197	Adrenoleukodystrophy	4.7%
198	Fabry Disease	4.6%
199	Jaw Abnormalities	4.6%
200	Cleft Palate	4.5%
201	Xeroderma Pigmentosum	4.5%
202	Amyloid Neuropathies, Familial	4.5%
203	Abnormalities, Radiation-Induced	4.5%
204	Hepatolenticular Degeneration	4.4%
205	Hydrops Fetalis	4.4%
206	Arthrogryposis	4.2%
207	Choanal Atresia	4.2%
208	Tracheobronchomegaly	4.2%
209	Laryngocele	4.2%
210	Aortic coarctation	4.2%
211	Cor Triatriatum	4.2%
212	Coronary Vessel Anomalies	4.2%
213	Dental Enamel Hypoplasia	4.2%
214	Patent ductus arteriosus	4.2%
215	Ebstein Anomaly	4.2%
216	Heart Septal Defects	4.2%
217	Hypodontia	4.2%
218	Macrostomia	4.2%
219	Meningocele	4.2%
220	Microstomia	4.2%
221	Tetralogy of Fallot	4.2%
222	Transposition of Great Vessels	4.2%
223	Hypoplastic Left Heart Syndrome	4.2%
224	May-Thurner Syndrome	4.2%
225	Encephalocele	4.2%
226	Choledochal Cyst	4.2%
227	Craniofacial Dysostosis	4.2%
228	Duane Retraction Syndrome	4.2%
229	Hermaphroditism	4.2%
230	Disorders of Sex Development	4.2%
231	Hypolipoproteinemias	4.1%
232	Papillon-Lefevre Disease	4.1%
233	Wolff-Parkinson-White Syndrome	4.1%
234	Hyperlipidemia, Familial Combined	4.1%
235	Cryptorchidism	4.1%
236	Porphyrias, Hepatic	4.1%
237	Hypospadias	4.1%
238	Hyperlipoproteinemia Type III	4.1%
239	Optic Atrophy, Hereditary, Leber	4.1%
240	Micrognathism	4.1%
241	Pierre Robin Syndrome	4.1%
242	Central Nervous System Cysts	4.1%
243	Hyperphosphaturia	4.1%
244	Gaucher Disease	4.1%
245	Dandy-Walker Syndrome	4.1%
246	Peutz-Jeghers Syndrome	4%
247	Myotonia Congenita	4%
248	Thrombasthenia	4%
249	Antithrombin III Deficiency	4%
250	Protein C Deficiency	4%
251	Brain Diseases, Metabolic, Inborn	4%
252	Afibrinogenemia	4%
253	Dystonia Musculorum Deformans	4%
254	Factor VII Deficiency	4%
255	Factor X Deficiency	4%
256	Factor XII Deficiency	4%
257	Hemophilia A	4%
258	POEMS Syndrome	4%
259	Activated Protein C Resistance	4%
260	Factor II deficiency	4%
261	Factor VIII Deficiency	4%
262	Factor V deficiency	4%
263	Factor XI Deficiency	4%
264	Hypoprothrombinemias	4%
265	Fanconi Anemia	4%
266	Basal Cell Nevus Syndrome	4%
267	Lafora Disease	4%
268	Unverricht-Lundborg Syndrome	4%
269	Anemia, Diamond-Blackfan	3.9%
270	Homocystinuria	3.9%
271	Leigh Disease	3.9%
272	Tay-Sachs Disease	3.9%
273	Canavan Disease	3.8%
274	Alexander Disease	3.8%
275	Aortopulmonary Septal Defect	3.7%
276	Double Outlet Right Ventricle	3.7%
277	Endocardial Cushion Defects	3.7%
278	Myocardial bridging	3.7%
279	Aorticopulmonary Septal Defect	3.7%
280	Hypoalphalipoproteinemias	3.7%
281	Carbamoyl-Phosphate Synthase I Deficiency Disease	3.6%
282	Retrognathia	3.6%
283	Niemann-Pick Disease, Type C	3.6%
284	Multiple Endocrine Neoplasia	3.5%
285	Laryngomalacia	3.5%
286	Truncus Arteriosus, Persistent	3.5%
287	Goldenhar Syndrome	3.5%
288	Pectus carinatum	3.4%
289	Ataxia Telangiectasia	3.4%
290	Bladder Exstrophy	3.4%
291	Congenital Hypothyroidism	3.4%
292	Epispadias	3.4%
293	Familial Periodic Paralysis	3.4%
294	Dermatitis, Atopic	3.4%
295	Multicystic Dysplastic Kidney	3.4%
296	Long QT Syndrome	3.4%
297	Platybasia	3.4%
298	Tricuspid Atresia	3.4%
299	Arrhythmogenic Right Ventricular Dysplasia	3.4%
300	Gonadal Dysgenesis	3.3%
301	Bronchomalacia	3.3%
302	Adrenogenital Syndrome	3.3%
303	Tracheomalacia	3.3%
304	Ovotesticular Disorders of Sex Development	3.3%
305	Lactose Intolerance	3.3%
306	Variegate Porphyria	3.3%
307	Acute intermittent porphyria	3.3%
308	Porphyria Cutanea Tarda	3.3%
309	Hyperhomocysteinemia	3.3%
310	Renal Aminoacidurias	3.3%
311	Fanconi Syndrome	3.3%
312	Pseudohypoaldosteronism	3.3%
313	Liddle Syndrome	3.3%
314	Hyperlipoproteinemia Type IV	3.3%
315	Hyperlipoproteinemia Type V	3.3%
316	Hyperandrogenism	3.2%
317	Prognathism	3.2%
318	Hypokalemic periodic paralysis	3%
319	Mandibulofacial Dysostosis	3%
320	Romano-Ward Syndrome	3%
321	Cystinuria	2.9%
322	Behcet Syndrome	2.9%
323	Talipes	2.8%
324	Gout	2.8%
325	Multiple Endocrine Neoplasia Type 1	2.8%
326	Pseudohypoparathyroidism	2.8%
327	Friedreich Ataxia	2.7%
328	Renal tubular acidosis	2.7%
329	Congenital clubfoot	2.7%
330	Vertical Talus	2.7%
331	Huntington Disease	2.5%
332	Arthritis, Gouty	2.5%
333	Denys-Drash Syndrome	2.4%
334	Familial Hypophosphatemic Rickets	2.2%
335	Nephroblastoma	2.2%
336	Arteriovenous fistula	2.1%
337	Glycosuria, Renal	2%
338	Adenomatous Polyposis Coli	2%
339	MELAS Syndrome	1.6%

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