MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Retinal Dysplasia

(UMLS:C0035313)

Definition:: Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
UMLS ID:: C0035313
MeSH ID:: D015792

Classification 1:

Name:

Eye Diseases
MeSH Tree Number(s):: C11.250.666|C11.270.660|C11.768.660

Classification 2:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.131.384.784|C16.320.290.660

Synonym(s)

Retinal Dysplasia

Retinal dysgenesis

Retinal dysplasia

Retinal dysplasia, NOS

dysplasia; retina

retina dysplasia

retina; dysplasia

retinal dysplasia

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Cytarabine		806125	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Aniridia	55.9%
2	Blepharophimosis	41.7%
3	Retinitis Pigmentosa	41.6%
4	Pigmentary retinopathy	41.6%
5	Retinal Degeneration	40%
6	Aicardi's syndrome	38.6%
7	Duane Retraction Syndrome	36.9%
8	Anophthalmos	35.6%
9	Microphthalmos	35.6%
10	CHARGE Syndrome	30.2%
11	Albinism	28.2%
12	Retinal Hemorrhage	27.7%
13	Alstrom Syndrome	25.2%
14	Retinoblastoma	24.6%
15	Chorioretinitis	24.4%
16	Retinopathy of Prematurity	23.8%
17	Angioid Streaks	23.3%
18	Retinal Detachment	23.3%
19	Retinitis	23.3%
20	Optic Atrophy, Hereditary, Leber	22.5%
21	Asthenopia	21.4%
22	Conjunctival Diseases	21.4%
23	Corneal Diseases	21.4%
24	Eyelid Diseases	21.4%
25	Lacrimal Apparatus Diseases	21.4%
26	Lens Diseases	21.4%
27	Ocular Hypertension	21.4%
28	Ocular Hypotension	21.4%
29	Scleral Diseases	21.4%
30	Vitreous Detachment	21.4%
31	Posterior Vitreous Detachment	21.4%
32	Uveal Neoplasms	20.9%
33	Xerophthalmia	20.8%
34	Low Tension Glaucoma	20.8%
35	Iridocorneal endothelial syndrome	20.8%
36	Eyelid Neoplasms	20.8%
37	Beckwith-Wiedemann Syndrome	20.5%
38	Wolf-Hirschhorn Syndrome	20.5%
39	Color blindness	20.4%
40	Keratoconjunctivitis Sicca	20.3%
41	Holoprosencephaly	20.2%
42	Retinal Artery Occlusion	19.8%
43	Retinal Vasculitis	19.8%
44	Hypertensive Retinopathy	19.8%
45	Retinal Neovascularization	19.7%
46	Retinal Dysplasia	19.4%
47	Eye Infection	18.4%
48	Eye Manifestations	18.4%
49	Eye Neoplasms	18.4%
50	Optic Neuropathy	18.4%
51	Smith-Magenis syndrome	18.3%
52	Cytomegalovirus Retinitis	18.3%
53	Corneal Scar	18.3%
54	Cri-du-Chat Syndrome	18.1%
55	Down Syndrome	18.1%
56	Trisomy 21	18.1%
57	Corneal Ulcer	18.1%
58	Choroid Hemorrhage	18%
59	Pars Planitis	18%
60	Keratoconjunctivitis	17.6%
61	Retinal Vein Occlusion	17.3%
62	Macular degeneration	17.2%
63	Retinal Drusen	17.2%
64	Retinal Necrosis Syndrome, Acute	17.2%
65	Retinoschisis	17.2%
66	Diabetic Retinopathy	17.2%
67	Rubinstein-Taybi Syndrome	16.8%
68	Kartagener Syndrome	16.7%
69	Trachoma	16.5%
70	Ectodermal Dysplasia	16.3%
71	Aplasia Cutis Congenita	16.3%
72	Prader-Willi Syndrome	16.2%
73	Ocular Motility Disorders	16.1%
74	Cyclophoria	16.1%
75	Fragile X Syndrome	16%
76	Hordeolum	16%
77	Pupil Disorders	15.9%
78	Eye Hemorrhage	15.8%
79	Vision Disorders	15.7%
80	Metamorphopsia	15.7%
81	Visual Impairment	15.7%
82	Eye Injuries	15.7%
83	Nail-Patella Syndrome	15.4%
84	Choroiditis	15.3%
85	Iridocyclitis	15.3%
86	Iritis	15.3%
87	Eye Abnormalities	15.3%
88	Ichthyosis, X-Linked	15.3%
89	Mandibulofacial Dysostosis	14.9%
90	Marfan Syndrome	14.8%
91	Cockayne Syndrome	14.8%
92	Retinal Diseases	14.3%
93	Cystic Fibrosis	14.1%
94	Abnormalities, Drug-Induced	14%
95	Anisometropia	14%
96	Aphakia	14%
97	Astigmatism	14%
98	Blepharitis	14%
99	Blepharoptosis	14%
100	Blepharospasm	14%
101	Choroid Diseases	14%
102	Conjunctivitis	14%
103	Corneal edema	14%
104	Corneal Opacity	14%
105	Dacryocystitis	14%
106	Dry Eye Syndromes	14%
107	Ectropion	14%
108	Enophthalmos	14%
109	Entropion	14%
110	Episcleritis	14%
111	Exophthalmos	14%
112	Glaucoma	14%
113	Iris Diseases	14%
114	Keratitis	14%
115	Keratoconus	14%
116	Lacrimal Duct Obstruction	14%
117	Lens dislocation	14%
118	Lens Subluxation	14%
119	Mydriasis	14%
120	Myopia	14%
121	Presbyopia	14%
122	Pterygium	14%
123	Scleritis	14%
124	Situs Inversus	14%
125	Uveitis	14%
126	Corneal Neovascularization	14%
127	Orbital Pseudotumor	14%
128	Cataract	14%
129	Pinguecula	14%
130	Trichiasis	14%
131	Acanthamoeba Keratitis	13.7%
132	Keratitis, Herpetic	13.7%
133	Bacterial conjunctivitis	13.6%
134	Corneal Perforation	13.5%
135	Congenital nystagmus	12.9%
136	Ophthalmia Neonatorum	12.8%
137	Panophthalmitis	12.4%
138	Neoplastic Syndromes, Hereditary	12.2%
139	Cardiovascular Abnormalities	12.2%
140	Smith-Lemli-Opitz Syndrome	12.2%
141	Anemia, Sickle Cell	12.1%
142	Thalassemia	12.1%
143	Muscular Dystrophy, Duchenne	12%
144	Polycystic Kidney Diseases	12%
145	Williams Syndrome	12%
146	Skin Abnormalities	12%
147	Lymphatic Abnormalities	12%
148	Congenital Microtia	12%
149	Anencephaly	11.9%
150	Endophthalmitis	11.9%
151	Multiple Epiphyseal Dysplasia	11.9%
152	Optic Atrophy	11.9%
153	Optic Neuritis	11.9%
154	Osteochondrodysplasias	11.9%
155	Papilledema	11.9%
156	Pelger-Huet Anomaly	11.9%
157	Pemphigoid, Benign Mucous Membrane	11.9%
158	Strabismus	11.9%
159	Tolosa-Hunt Syndrome	11.9%
160	Werner Syndrome	11.9%
161	Orbital Cellulitis	11.9%
162	Retrobulbar Hemorrhage	11.9%
163	Myasthenic Syndromes, Congenital	11.9%
164	Corneal Endothelial Cell Loss	11.9%
165	Hyphema	11.8%
166	Vitreous Hemorrhage	11.8%
167	Congenital diaphragmatic hernia	11.8%
168	Mucopolysaccharidosis II	11.2%
169	Primary Ciliary Dyskinesia	11.1%
170	Sjogren-Larsson Syndrome	10.9%
171	Epidermolysis Bullosa	10.9%
172	Urogenital Abnormalities	10.7%
173	Xeroderma	10.7%
174	Mobius Syndrome	10.7%
175	Maxillofacial Abnormalities	10.6%
176	Dural Arteriovenous Fistula	10.6%
177	Dwarfism	10.6%
178	Menkes Kinky Hair Syndrome	10.6%
179	Dextrocardia	10.6%
180	Optic Neuropathy, Ischemic	10.4%
181	Anterior Ischemic Optic Neuropathy	10.4%
182	Kallmann Syndrome	10.4%
183	Angle Closure Glaucoma	10.3%
184	Glaucoma, Open-Angle	10.3%
185	Panuveitis	10.3%
186	Exfoliation Syndrome	10.3%
187	Classical Lissencephalies and Subcortical Band Heterotopias	10.3%
188	Anisocoria	10.3%
189	Muscular Dystrophy	10.3%
190	Osteogenesis Imperfecta	10.3%
191	Tonic Pupil	10.3%
192	Eye pain	10.3%
193	Orbital Myositis	10.3%
194	Tuberous Sclerosis	10.3%
195	Diplopia	10.2%
196	Scotoma	10.2%
197	Photophobia	10.2%
198	Amaurosis	10.2%
199	Blindness	10.2%
200	Fetal Diseases	10.2%
201	Rett Syndrome	10.1%
202	Refsum Disease	9.9%
203	Wiskott-Aldrich Syndrome	9.8%
204	Turner Syndrome	9.5%
205	Autoimmune Lymphoproliferative Syndrome	9.2%
206	Familial Mediterranean Fever	9.2%
207	Prune Belly Syndrome	9.2%
208	Twins, Conjoined	9.2%
209	Waardenburg Syndrome	9.2%
210	Ophthalmoplegia	9.1%
211	External Ophthalmoplegia	9.1%
212	Behcet Syndrome	9.1%
213	Amblyopia	9.1%
214	Pseudoxanthoma Elasticum	9.1%
215	Angioedemas, Hereditary	9.1%
216	Adrenoleukodystrophy	9%
217	Myotonic Dystrophy	9%
218	Sickle Cell Trait	8.9%
219	Polycystic Kidney, Autosomal Dominant	8.9%
220	Zellweger Syndrome	8.9%
221	Esotropia	8.8%
222	Exotropia	8.8%
223	Choroidal Neovascularization	8.8%
224	Scimitar Syndrome	8.8%
225	Acrocephalosyndactylia	8.7%
226	Neuronal Ceroid-Lipofuscinoses	8.7%
227	Anterior uveitis	8.6%
228	Uveitis, Posterior	8.6%
229	Hyperkeratosis, Epidermolytic	8.4%
230	Xeroderma Pigmentosum	8.4%
231	Hepatolenticular Degeneration	8.3%
232	Meconium Aspiration Syndrome	8.3%
233	Klinefelter Syndrome	8.3%
234	Kearns-Sayre syndrome	8.2%
235	Fabry Disease	8.2%
236	Microcephaly	8.2%
237	Macrocephaly	8.2%
238	Abnormalities, Radiation-Induced	8.2%
239	Craniosynostosis	8.1%
240	Syndactyly	8.1%
241	Brachycephaly	8.1%
242	Charcot-Marie-Tooth Disease	8%
243	Antley-Bixler Syndrome Phenotype	8%
244	Anus, Imperforate	7.9%
245	Hydranencephaly	7.9%
246	Neural Tube Defects	7.9%
247	Tethered Cord Syndrome	7.9%
248	Iniencephaly	7.9%
249	Craniorachischisis	7.9%
250	Limb Deformities, Congenital	7.9%
251	Exencephaly	7.9%
252	Septo-Optic Dysplasia	7.9%
253	Craniofacial Abnormalities	7.9%
254	Cortical Dysplasia	7.9%
255	Malformations of Cortical Development	7.9%
256	Anorectal Malformations	7.9%
257	Amino Acid Metabolism, Inborn Errors	7.8%
258	Bloom Syndrome	7.8%
259	Carbohydrate Metabolism, Inborn Errors	7.8%
260	Metal Metabolism, Inborn Errors	7.8%
261	Progeria	7.8%
262	Lysosomal Storage Diseases	7.8%
263	Cytochrome-c Oxidase Deficiency	7.8%
264	Peroxisomal Disorders	7.8%
265	Amyloid Neuropathies, Familial	7.8%
266	Uveomeningoencephalitic Syndrome	7.8%
267	Herpes Zoster Ophthalmicus	7.7%
268	Basal Cell Nevus Syndrome	7.6%
269	Hemianopsia	7.6%
270	Amaurosis Fugax	7.6%
271	Blindness, Cortical	7.6%
272	Glycogen storage disease type II	7.6%
273	Porencephaly	7.4%
274	Noonan Syndrome	7.4%
275	Acute Chest Syndrome	7.4%
276	Cleft Palate	7.4%
277	Galactosemias	7.3%
278	Urea Cycle Disorders, Inborn	7.3%
279	Tyrosinemias	7.3%
280	Abdominal Cramps	7%
281	Amniotic Band Syndrome	7%
282	Asphyxia Neonatorum	7%
283	Infant, Premature, Diseases	7%
284	Infantile Colic	7%
285	Laryngostenosis	7%
286	Mouth Abnormalities	7%
287	Cutis Laxa	6.9%
288	Esophageal Atresia	6.9%
289	Intestinal Atresia	6.9%
290	Horseshoe Kidney	6.9%
291	Pectus excavatum	6.9%
292	Graves Disease	6.9%
293	Klippel-Feil Syndrome	6.9%
294	Gastroschisis	6.9%
295	Synostosis	6.9%
296	Acrodermatitis	6.8%
297	Lymphangiectasis, Intestinal	6.8%
298	Porokeratosis	6.8%
299	Gianotti-Crosti Syndrome	6.8%
300	Keratoderma, Palmoplantar	6.8%
301	Ataxia Telangiectasia	6.8%
302	Chronic granulomatous disease	6.8%
303	Horner Syndrome	6.8%
304	Jaw Abnormalities	6.8%
305	Opsoclonus-Myoclonus Syndrome	6.8%
306	Welander Distal Myopathy	6.8%
307	Poland Syndrome	6.7%
308	Mucopolysaccharidosis III	6.6%
309	Hyperphosphaturia	6.6%
310	Canavan Disease	6.6%
311	Alexander Disease	6.6%
312	Gaucher Disease	6.3%
313	Arthrogryposis	6.2%
314	Choanal Atresia	6.2%
315	Tracheobronchomegaly	6.2%
316	Laryngocele	6.2%
317	Miller Fisher Syndrome	6.2%
318	Choledochal Cyst	6.2%
319	Hermaphroditism	6.2%
320	Disorders of Sex Development	6.2%
321	Homocystinuria	6.1%
322	Cryptorchidism	6.1%
323	Porphyrias, Hepatic	6.1%
324	Hypospadias	6.1%
325	Leigh Disease	6.1%
326	Central Nervous System Cysts	6.1%
327	Dandy-Walker Syndrome	6.1%
328	Peutz-Jeghers Syndrome	6%
329	Myotonia Congenita	6%
330	Thrombasthenia	6%
331	Antithrombin III Deficiency	6%
332	Protein C Deficiency	6%
333	Brain Diseases, Metabolic, Inborn	6%
334	Afibrinogenemia	6%
335	Dystonia Musculorum Deformans	6%
336	Factor VII Deficiency	6%
337	Factor X Deficiency	6%
338	Factor XII Deficiency	6%
339	Hemophilia A	6%
340	POEMS Syndrome	6%
341	Activated Protein C Resistance	6%
342	Factor II deficiency	6%
343	Factor VIII Deficiency	6%
344	Factor V deficiency	6%
345	Factor XI Deficiency	6%
346	Hypoprothrombinemias	6%
347	Fanconi Anemia	6%
348	Lafora Disease	6%
349	Unverricht-Lundborg Syndrome	6%
350	Anemia, Diamond-Blackfan	6%
351	Deformity	6%
352	Genetic Diseases, Inborn	6%
353	Anemia, Neonatal	5.9%
354	Persistent Fetal Circulation Syndrome	5.9%
355	Umbilical hernia	5.9%
356	Amelia	5.9%
357	Arachnodactyly	5.9%
358	Ectopia Cordis	5.9%
359	Ectromelia	5.9%
360	Hemimelia	5.9%
361	Meningomyelocele	5.9%
362	Phocomelia	5.9%
363	Sirenomelia	5.9%
364	Spina Bifida	5.9%
365	Polydactyly	5.9%
366	Brachydactyly	5.9%
367	Plagiocephaly	5.9%
368	Lower Extremity Deformities, Congenital	5.9%
369	Upper Extremity Deformities, Congenital	5.9%
370	Single umbilical artery	5.9%
371	Alkaptonuria	5.8%
372	Glycogen Storage Disease	5.8%
373	Hypophosphatasia	5.8%
374	Propionic acidemia	5.8%
375	Dihydropyrimidine Dehydrogenase Deficiency	5.8%
376	Cystinosis	5.8%
377	Micrognathism	5.8%
378	Pierre Robin Syndrome	5.8%
379	Tay-Sachs Disease	5.7%
380	Multiple Endocrine Neoplasia	5.6%
381	Laryngomalacia	5.6%
382	Pectus carinatum	5.5%
383	Niemann-Pick Disease, Type C	5.5%
384	Carbamoyl-Phosphate Synthase I Deficiency Disease	5.5%
385	Sicca Syndrome	5.5%
386	Sjogren's Syndrome	5.5%
387	Bladder Exstrophy	5.5%
388	Congenital Hypothyroidism	5.5%
389	Epispadias	5.5%
390	Dermatitis, Atopic	5.4%
391	Multicystic Dysplastic Kidney	5.4%
392	Retrognathia	5.3%
393	Neonatal Abstinence Syndrome	5.3%
394	Fetal Growth Retardation	5.2%
395	Fetal Hypoxia	5.2%
396	Fetal Alcohol Spectrum Disorders	5.2%
397	Toxoplasmosis, Congenital	5.1%
398	Aortic coarctation	5.1%
399	Cor Triatriatum	5.1%
400	Coronary Vessel Anomalies	5.1%
401	Dental Enamel Hypoplasia	5.1%
402	Patent ductus arteriosus	5.1%
403	Ebstein Anomaly	5.1%
404	Heart Septal Defects	5.1%
405	Hypodontia	5.1%
406	Macrostomia	5.1%
407	Meningocele	5.1%
408	Microstomia	5.1%
409	Syphilis, Congenital	5.1%
410	Tetralogy of Fallot	5.1%
411	Transposition of Great Vessels	5.1%
412	Hypoplastic Left Heart Syndrome	5.1%
413	May-Thurner Syndrome	5.1%
414	Encephalocele	5.1%
415	Craniofacial Dysostosis	5.1%
416	Hyperandrogenism	5.1%
417	Ophthalmoplegic Migraine	5.1%
418	Hypolipoproteinemias	5.1%
419	Papillon-Lefevre Disease	5.1%
420	Wolff-Parkinson-White Syndrome	5.1%
421	Hydrops Fetalis	5.1%
422	Hyperlipidemia, Familial Combined	5.1%
423	Hyperlipoproteinemia Type III	5%
424	Progressive supranuclear palsy	5%
425	Prognathism	4.9%
426	Dermal Sinus	4.8%
427	Spina Bifida Cystica	4.8%
428	Spina Bifida Occulta	4.8%
429	Lissencephaly	4.8%
430	Polymicrogyria	4.8%
431	Pachygyria	4.8%
432	Schizencephaly	4.8%
433	Periventricular Nodular Heterotopia	4.8%
434	Glycogen Storage Disease Type I	4.8%
435	Glycogen Storage Disease Type V	4.8%
436	Neuromyelitis Optica	4.6%
437	Congenital Hyperinsulinism	4.6%
438	Chorioamnionitis	4.6%
439	Familial Periodic Paralysis	4.5%
440	Long QT Syndrome	4.5%
441	Platybasia	4.5%
442	Tricuspid Atresia	4.5%
443	Arrhythmogenic Right Ventricular Dysplasia	4.5%
444	Gonadal Dysgenesis	4.5%
445	Bronchomalacia	4.5%
446	Adrenogenital Syndrome	4.5%
447	Tracheomalacia	4.5%
448	Ovotesticular Disorders of Sex Development	4.5%
449	Lactose Intolerance	4.5%
450	Variegate Porphyria	4.5%
451	Acute intermittent porphyria	4.5%
452	Porphyria Cutanea Tarda	4.5%
453	Hyperhomocysteinemia	4.5%
454	Huntington Disease	4.5%
455	Renal Aminoacidurias	4.5%
456	Fanconi Syndrome	4.5%
457	Pseudohypoaldosteronism	4.5%
458	Liddle Syndrome	4.5%
459	Hyperlipoproteinemia Type IV	4.5%
460	Hyperlipoproteinemia Type V	4.5%
461	Denys-Drash Syndrome	4.2%
462	Aortopulmonary Septal Defect	4.2%
463	Double Outlet Right Ventricle	4.2%
464	Endocardial Cushion Defects	4.2%
465	Myocardial bridging	4.2%
466	Aorticopulmonary Septal Defect	4.2%
467	Hypoalphalipoproteinemias	4.2%
468	Nephroblastoma	4.1%
469	Gout	4.1%
470	Multiple Endocrine Neoplasia Type 1	4.1%
471	Pseudohypoparathyroidism	4.1%
472	Friedreich Ataxia	4%
473	Renal tubular acidosis	4%
474	Paralysis, Obstetric	4%
475	Optic Nerve Glioma	3.9%
476	Bronchopulmonary Dysplasia	3.9%
477	Familial Hypophosphatemic Rickets	3.8%
478	Adenomatous Polyposis Coli	3.8%
479	Truncus Arteriosus, Persistent	3.8%
480	Goldenhar Syndrome	3.8%
481	Hypokalemic periodic paralysis	3.7%
482	Romano-Ward Syndrome	3.7%
483	Cystinuria	3.7%
484	Respiratory Distress Syndrome, Newborn	3.5%
485	Talipes	3.4%
486	Arthritis, Gouty	3.3%
487	Glycosuria, Renal	3.3%
488	Congenital clubfoot	3.2%
489	Vertical Talus	3.2%
490	Arteriovenous fistula	3%
491	Leukomalacia, Periventricular	3%
492	Nesidioblastosis	3%
493	MELAS Syndrome	2.8%
494	Hyaline Membrane Disease	2.6%
495	Kernicterus	2.5%

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