MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Amniotic Band Syndrome

(UMLS:C0002636)

Definition:: A disorder present in the newborn infant in which constriction rings or bands, causing soft tissue depressions, encircle digits, extremities, or limbs and sometimes the neck, thorax, or abdomen. They may be associated with intrauterine amputations.
UMLS ID:: C0002636
MeSH ID:: D000652

Classification:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.614.042

Synonym(s)

Amniotic Band Syndrome

AMNIOTIC BAND SYNDROME

Amniotic Band Constriction

Amniotic band anomalad

Amniotic band syndrome

Deformity due to Amniotic Band

amniotic band syndrome

Associated Drug(s)

	Name	Number of Reports	Data Source
1	Levetiracetam	FAERS: 8	US FAERS
2	Quetiapine Fumarate	FAERS: 4	US FAERS
3	Quetiapine Fumarate	FAERS: 4	US FAERS
4	Naproxen	FAERS: 3	US FAERS
5	Ondansetron	FAERS: 3	US FAERS
6	Paroxetine	FAERS: 3	US FAERS
7	Carbamazepine	FAERS: 2	US FAERS
8	Fluoxetine	FAERS: 2	US FAERS
9	Olanzapine	FAERS: 2	US FAERS
10	Diclofenac Sodium and Misoprostol	FAERS: 1	US FAERS
11	Fingolimod Hydrochloride	FAERS: 1	US FAERS
12	Tacrolimus	FAERS: 1	US FAERS
13	Aminocaproic Acid		OFFSIDES
14	Dicyclomine		OFFSIDES
15	Dimenhydrinate	Canada Vigilance: 1	Canada Vigilance
16	Nelfinavir		OFFSIDES
17	Norfloxacin		OFFSIDES
18	Rilmenidine		OFFSIDES
19	Zidovudine		OFFSIDES
20	efavirenz		OFFSIDES
21	lamivudine, zidovudine drug combination		OFFSIDES

Similar ADE(s)

	Name	Semantic Similarity
1	Abdominal Cramps	42.9%
2	Asphyxia Neonatorum	42.9%
3	Infant, Premature, Diseases	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	Retinopathy of Prematurity	20.9%
14	Xeroderma	20.5%
15	Mobius Syndrome	20.5%
16	Congenital nystagmus	20.5%
17	Toxoplasmosis, Congenital	20.3%
18	Bronchopulmonary Dysplasia	20.2%
19	Syphilis, Congenital	20.2%
20	Meconium Aspiration Syndrome	18.6%
21	Congenital Hyperinsulinism	16.4%
22	Respiratory Distress Syndrome, Newborn	15.8%
23	Beckwith-Wiedemann Syndrome	15.3%
24	Wolf-Hirschhorn Syndrome	15.3%
25	Fetal Diseases	15%
26	Abnormalities, Drug-Induced	14.3%
27	Situs Inversus	14.3%
28	Ichthyosis, X-Linked	13.2%
29	Hyaline Membrane Disease	12.6%
30	Smith-Magenis syndrome	12.3%
31	Aicardi's syndrome	12.2%
32	Cri-du-Chat Syndrome	12.1%
33	Down Syndrome	12.1%
34	Trisomy 21	12.1%
35	CHARGE Syndrome	12.1%
36	Leukomalacia, Periventricular	12%
37	Nesidioblastosis	11.9%
38	Holoprosencephaly	11.7%
39	Hyperkeratosis, Epidermolytic	11.4%
40	Ophthalmia Neonatorum	11.3%
41	Sjogren-Larsson Syndrome	11%
42	Fragile X Syndrome	10.9%
43	Familial Mediterranean Fever	10.3%
44	Prune Belly Syndrome	10.3%
45	Twins, Conjoined	10.3%
46	Waardenburg Syndrome	10.3%
47	Ectodermal Dysplasia	10.1%
48	Aplasia Cutis Congenita	10.1%
49	Eye Abnormalities	10%
50	Neoplastic Syndromes, Hereditary	10%
51	Prader-Willi Syndrome	10%
52	Cardiovascular Abnormalities	10%
53	Nail-Patella Syndrome	9.7%
54	Rubinstein-Taybi Syndrome	9.5%
55	Skin Abnormalities	9.5%
56	Lymphatic Abnormalities	9.5%
57	Congenital Microtia	9.5%
58	Multiple Epiphyseal Dysplasia	9.3%
59	Osteochondrodysplasias	9.3%
60	Pelger-Huet Anomaly	9.3%
61	Werner Syndrome	9.3%
62	Myasthenic Syndromes, Congenital	9.3%
63	Anencephaly	9.2%
64	Congenital diaphragmatic hernia	9.2%
65	Kernicterus	8.7%
66	Cockayne Syndrome	8.6%
67	Alstrom Syndrome	8.5%
68	Kartagener Syndrome	8.5%
69	Rett Syndrome	8.2%
70	Marfan Syndrome	8.1%
71	Primary Ciliary Dyskinesia	8%
72	Anemia, Sickle Cell	8%
73	Thalassemia	8%
74	Muscular Dystrophy, Duchenne	8%
75	Polycystic Kidney Diseases	8%
76	Williams Syndrome	8%
77	Smith-Lemli-Opitz Syndrome	7.5%
78	Maxillofacial Abnormalities	7.5%
79	Dural Arteriovenous Fistula	7.5%
80	Classical Lissencephalies and Subcortical Band Heterotopias	7.4%
81	Urogenital Abnormalities	7.4%
82	Dextrocardia	7.4%
83	Dwarfism	7.3%
84	Albinism	7.1%
85	Anophthalmos	7%
86	Anus, Imperforate	7%
87	Hydranencephaly	7%
88	Microphthalmos	7%
89	Neural Tube Defects	7%
90	Retinal Dysplasia	7%
91	Tethered Cord Syndrome	7%
92	Iniencephaly	7%
93	Craniorachischisis	7%
94	Limb Deformities, Congenital	7%
95	Exencephaly	7%
96	Septo-Optic Dysplasia	7%
97	Craniofacial Abnormalities	7%
98	Cortical Dysplasia	7%
99	Malformations of Cortical Development	7%
100	Anorectal Malformations	7%
101	Aniridia	6.9%
102	Fetal Growth Retardation	6.9%
103	Muscular Dystrophy	6.8%
104	Osteogenesis Imperfecta	6.8%
105	Fetal Hypoxia	6.8%
106	Fetal Alcohol Spectrum Disorders	6.8%
107	Mucopolysaccharidosis II	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	Progeria	6.8%
113	Lysosomal Storage Diseases	6.8%
114	Cytochrome-c Oxidase Deficiency	6.8%
115	Peroxisomal Disorders	6.8%
116	Epidermolysis Bullosa	6.7%
117	Sickle Cell Trait	6.5%
118	Polycystic Kidney, Autosomal Dominant	6.5%
119	Microcephaly	6.3%
120	Macrocephaly	6.3%
121	Kallmann Syndrome	5.9%
122	Menkes Kinky Hair Syndrome	5.9%
123	Porencephaly	5.9%
124	Neuronal Ceroid-Lipofuscinoses	5.8%
125	Wiskott-Aldrich Syndrome	5.7%
126	Tuberous Sclerosis	5.6%
127	Amelia	5.6%
128	Arachnodactyly	5.6%
129	Ectopia Cordis	5.6%
130	Ectromelia	5.6%
131	Hemimelia	5.6%
132	Meningomyelocele	5.6%
133	Phocomelia	5.6%
134	Sirenomelia	5.6%
135	Spina Bifida	5.6%
136	Polydactyly	5.6%
137	Brachydactyly	5.6%
138	Plagiocephaly	5.6%
139	Lower Extremity Deformities, Congenital	5.6%
140	Upper Extremity Deformities, Congenital	5.6%
141	Single umbilical artery	5.6%
142	Alkaptonuria	5.6%
143	Glycogen Storage Disease	5.6%
144	Hypophosphatasia	5.6%
145	Propionic acidemia	5.6%
146	Autoimmune Lymphoproliferative Syndrome	5.6%
147	Dihydropyrimidine Dehydrogenase Deficiency	5.6%
148	Cystinosis	5.6%
149	Craniosynostosis	5.5%
150	Syndactyly	5.5%
151	Brachycephaly	5.5%
152	Klinefelter Syndrome	5.5%
153	Charcot-Marie-Tooth Disease	5.5%
154	Antley-Bixler Syndrome Phenotype	5.5%
155	Chorioamnionitis	5.4%
156	Refsum Disease	5.4%
157	Scimitar Syndrome	5.4%
158	Angioedemas, Hereditary	5.4%
159	Turner Syndrome	5.3%
160	Acrocephalosyndactylia	5.3%
161	Blepharophimosis	5.3%
162	Laryngostenosis	5.3%
163	Mouth Abnormalities	5.3%
164	Cutis Laxa	5.2%
165	Esophageal Atresia	5.2%
166	Intestinal Atresia	5.2%
167	Horseshoe Kidney	5.2%
168	Pectus excavatum	5.2%
169	Klippel-Feil Syndrome	5.1%
170	Retinitis Pigmentosa	5.1%
171	Gastroschisis	5.1%
172	Synostosis	5.1%
173	Pigmentary retinopathy	5.1%
174	Acrodermatitis	5.1%
175	Lymphangiectasis, Intestinal	5.1%
176	Porokeratosis	5.1%
177	Gianotti-Crosti Syndrome	5.1%
178	Keratoderma, Palmoplantar	5.1%
179	Pseudoxanthoma Elasticum	5.1%
180	Chronic granulomatous disease	5%
181	Welander Distal Myopathy	5%
182	Dermal Sinus	5%
183	Spina Bifida Cystica	5%
184	Spina Bifida Occulta	5%
185	Lissencephaly	5%
186	Polymicrogyria	5%
187	Pachygyria	5%
188	Schizencephaly	5%
189	Periventricular Nodular Heterotopia	5%
190	Myotonic Dystrophy	5%
191	Glycogen Storage Disease Type I	4.9%
192	Glycogen Storage Disease Type V	4.9%
193	Poland Syndrome	4.9%
194	Mucopolysaccharidosis III	4.9%
195	Glycogen storage disease type II	4.8%
196	Noonan Syndrome	4.8%
197	Zellweger Syndrome	4.8%
198	Acute Chest Syndrome	4.8%
199	Galactosemias	4.7%
200	Urea Cycle Disorders, Inborn	4.7%
201	Tyrosinemias	4.7%
202	Adrenoleukodystrophy	4.7%
203	Fabry Disease	4.6%
204	Jaw Abnormalities	4.6%
205	Cleft Palate	4.5%
206	Xeroderma Pigmentosum	4.5%
207	Amyloid Neuropathies, Familial	4.5%
208	Abnormalities, Radiation-Induced	4.5%
209	Hepatolenticular Degeneration	4.4%
210	Hydrops Fetalis	4.4%
211	Arthrogryposis	4.2%
212	Choanal Atresia	4.2%
213	Tracheobronchomegaly	4.2%
214	Laryngocele	4.2%
215	Aortic coarctation	4.2%
216	Cor Triatriatum	4.2%
217	Coronary Vessel Anomalies	4.2%
218	Dental Enamel Hypoplasia	4.2%
219	Patent ductus arteriosus	4.2%
220	Ebstein Anomaly	4.2%
221	Heart Septal Defects	4.2%
222	Hypodontia	4.2%
223	Macrostomia	4.2%
224	Meningocele	4.2%
225	Microstomia	4.2%
226	Tetralogy of Fallot	4.2%
227	Transposition of Great Vessels	4.2%
228	Hypoplastic Left Heart Syndrome	4.2%
229	May-Thurner Syndrome	4.2%
230	Encephalocele	4.2%
231	Choledochal Cyst	4.2%
232	Craniofacial Dysostosis	4.2%
233	Duane Retraction Syndrome	4.2%
234	Hermaphroditism	4.2%
235	Disorders of Sex Development	4.2%
236	Hypolipoproteinemias	4.1%
237	Papillon-Lefevre Disease	4.1%
238	Wolff-Parkinson-White Syndrome	4.1%
239	Hyperlipidemia, Familial Combined	4.1%
240	Cryptorchidism	4.1%
241	Porphyrias, Hepatic	4.1%
242	Hypospadias	4.1%
243	Hyperlipoproteinemia Type III	4.1%
244	Optic Atrophy, Hereditary, Leber	4.1%
245	Micrognathism	4.1%
246	Pierre Robin Syndrome	4.1%
247	Central Nervous System Cysts	4.1%
248	Hyperphosphaturia	4.1%
249	Gaucher Disease	4.1%
250	Dandy-Walker Syndrome	4.1%
251	Peutz-Jeghers Syndrome	4%
252	Myotonia Congenita	4%
253	Thrombasthenia	4%
254	Antithrombin III Deficiency	4%
255	Protein C Deficiency	4%
256	Brain Diseases, Metabolic, Inborn	4%
257	Afibrinogenemia	4%
258	Dystonia Musculorum Deformans	4%
259	Factor VII Deficiency	4%
260	Factor X Deficiency	4%
261	Factor XII Deficiency	4%
262	Hemophilia A	4%
263	POEMS Syndrome	4%
264	Activated Protein C Resistance	4%
265	Factor II deficiency	4%
266	Factor VIII Deficiency	4%
267	Factor V deficiency	4%
268	Factor XI Deficiency	4%
269	Hypoprothrombinemias	4%
270	Fanconi Anemia	4%
271	Basal Cell Nevus Syndrome	4%
272	Lafora Disease	4%
273	Unverricht-Lundborg Syndrome	4%
274	Anemia, Diamond-Blackfan	3.9%
275	Homocystinuria	3.9%
276	Leigh Disease	3.9%
277	Tay-Sachs Disease	3.9%
278	Canavan Disease	3.8%
279	Alexander Disease	3.8%
280	Aortopulmonary Septal Defect	3.7%
281	Double Outlet Right Ventricle	3.7%
282	Endocardial Cushion Defects	3.7%
283	Myocardial bridging	3.7%
284	Aorticopulmonary Septal Defect	3.7%
285	Hypoalphalipoproteinemias	3.7%
286	Carbamoyl-Phosphate Synthase I Deficiency Disease	3.6%
287	Retrognathia	3.6%
288	Niemann-Pick Disease, Type C	3.6%
289	Multiple Endocrine Neoplasia	3.5%
290	Laryngomalacia	3.5%
291	Truncus Arteriosus, Persistent	3.5%
292	Goldenhar Syndrome	3.5%
293	Pectus carinatum	3.4%
294	Ataxia Telangiectasia	3.4%
295	Bladder Exstrophy	3.4%
296	Congenital Hypothyroidism	3.4%
297	Epispadias	3.4%
298	Familial Periodic Paralysis	3.4%
299	Dermatitis, Atopic	3.4%
300	Multicystic Dysplastic Kidney	3.4%
301	Long QT Syndrome	3.4%
302	Platybasia	3.4%
303	Tricuspid Atresia	3.4%
304	Arrhythmogenic Right Ventricular Dysplasia	3.4%
305	Gonadal Dysgenesis	3.3%
306	Bronchomalacia	3.3%
307	Adrenogenital Syndrome	3.3%
308	Tracheomalacia	3.3%
309	Ovotesticular Disorders of Sex Development	3.3%
310	Lactose Intolerance	3.3%
311	Variegate Porphyria	3.3%
312	Acute intermittent porphyria	3.3%
313	Porphyria Cutanea Tarda	3.3%
314	Hyperhomocysteinemia	3.3%
315	Renal Aminoacidurias	3.3%
316	Fanconi Syndrome	3.3%
317	Pseudohypoaldosteronism	3.3%
318	Liddle Syndrome	3.3%
319	Hyperlipoproteinemia Type IV	3.3%
320	Hyperlipoproteinemia Type V	3.3%
321	Hyperandrogenism	3.2%
322	Prognathism	3.2%
323	Hypokalemic periodic paralysis	3%
324	Mandibulofacial Dysostosis	3%
325	Romano-Ward Syndrome	3%
326	Cystinuria	2.9%
327	Behcet Syndrome	2.9%
328	Talipes	2.8%
329	Gout	2.8%
330	Multiple Endocrine Neoplasia Type 1	2.8%
331	Pseudohypoparathyroidism	2.8%
332	Friedreich Ataxia	2.7%
333	Renal tubular acidosis	2.7%
334	Congenital clubfoot	2.7%
335	Vertical Talus	2.7%
336	Huntington Disease	2.5%
337	Arthritis, Gouty	2.5%
338	Denys-Drash Syndrome	2.4%
339	Familial Hypophosphatemic Rickets	2.2%
340	Nephroblastoma	2.2%
341	Arteriovenous fistula	2.1%
342	Glycosuria, Renal	2%
343	Adenomatous Polyposis Coli	2%
344	MELAS Syndrome	1.6%

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