MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Arthritis, Gouty

(UMLS:C0003868)

Definition:: Arthritis, especially of the great toe, as a result of gout. Acute gouty arthritis often is precipitated by trauma, infection, surgery, etc. The initial attacks are usually monoarticular but later attacks are often polyarticular. Acute and chronic gouty arthritis are associated with accumulation of MONOSODIUM URATE in and around affected joints.
UMLS ID:: C0003868
MeSH ID:: D015210

Classification 1:

Name:

Musculoskeletal Diseases
MeSH Tree Number(s):: C05.550.114.423.410|C05.550.354.500.500|C05.799.414.410

Classification 2:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.320.565.798.368.410

Classification 3:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.648.798.368.410

Synonym(s)

Arthritis, Gouty

ARTHRITIS GOUT

ARTHRITIS, GOUTY

ARTHROPATHY GOUT

Arthritis due to gout

Articular gout

Articular gout, NOS

Gouty Arthritis

Gouty arthritis

10.

Gouty arthritis, NOS

11.

Gouty arthropathy

12.

Gouty arthropathy, unspecified

13.

Joints gout affected

14.

arthritis gout

15.

arthritis gouty

16.

arthritis; gout

17.

arthritis; uratic

18.

arthropathy gout

19.

arthropathy; gouty

20.

gout arthritis

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Acetaminophen	17276548	CTD
2	Allopurinol	5655316 17013833	CTD
3	Benzbromarone	17013833	CTD
4	Colchicine	View details 3701734 5655316 14713183 17497454 20661070	CTD
5	Diclofenac	15975301	CTD
6	Indomethacin	6023116 17276548	CTD
7	Phenylbutazone	5655316	CTD
8	Prednisolone	17276548	CTD
9	Probenecid	3701734 5655316	CTD
10	Sulfinpyrazone	9587090	CTD
11	Uric Acid	19655406	CTD
12	lithospermic acid	18694741	CTD
13	paederosidic acid methyl ester	19655406	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Arthrogryposis	26.2%
2	Periarthritis	26%
3	Rheumatic Fever	25.4%
4	Osteoarthritis, Spine	25%
5	Contracture	24.6%
6	Osteoarthropathy, Secondary Hypertrophic	24.6%
7	Rheumatoid Arthritis	22.9%
8	Juvenile arthritis	22.9%
9	Metatarsalgia	21.5%
10	Dihydropyrimidine Dehydrogenase Deficiency	20.7%
11	Arthritis, Psoriatic	20.1%
12	Bursitis	19.7%
13	Joint Instability	19.7%
14	Synovitis	19.7%
15	Joint laxity	19.7%
16	Frozen shoulder	19.7%
17	Patellofemoral Pain Syndrome	19.7%
18	Nail-Patella Syndrome	19.2%
19	Osteoarthritis, Knee	19%
20	Sacroiliitis	18.4%
21	Fibromyalgia	18.3%
22	Polymyalgia Rheumatica	18.3%
23	Ankylosing spondylitis	17.8%
24	Temporomandibular Joint Disorders	17.7%
25	Hemarthrosis	16.9%
26	Rheumatoid Nodule	16.6%
27	Amino Acid Metabolism, Inborn Errors	16.3%
28	Carbohydrate Metabolism, Inborn Errors	16.3%
29	Metal Metabolism, Inborn Errors	16.3%
30	Progeria	16.3%
31	Lysosomal Storage Diseases	16.3%
32	Peroxisomal Disorders	16.3%
33	Arthritis, Reactive	16.2%
34	Arthritis, Infectious	16%
35	Arthritis, Experimental	15.8%
36	Bone Diseases	15.6%
37	Fasciitis	15.6%
38	Foot Deformities	15.6%
39	Brain Diseases, Metabolic, Inborn	15.4%
40	Ischemic contracture	15.3%
41	Fasciitis, Plantar	15.2%
42	Pseudohypoparathyroidism	15%
43	Hip Contracture	14.9%
44	Felty Syndrome	14.8%
45	Pectus carinatum	14.8%
46	Smith-Lemli-Opitz Syndrome	14.4%
47	Osteopenia	14%
48	Jaw Diseases	13.8%
49	Galactosemias	13.6%
50	Urea Cycle Disorders, Inborn	13.6%
51	Tyrosinemias	13.6%
52	Cartilage Diseases	13.5%
53	Foot Diseases	13.5%
54	Myopathy	13.5%
55	Chondromalacia	13.5%
56	Familial Periodic Paralysis	13.5%
57	Rheumatoid Vasculitis	13.3%
58	Osteochondritis	13.3%
59	Temporomandibular Joint Dysfunction Syndrome	13.2%
60	Spondylarthropathies	13.1%
61	Arthralgia	13%
62	Polyarthralgia	13%
63	Leigh Disease	12.6%
64	Hyperphosphaturia	12.5%
65	Antley-Bixler Syndrome Phenotype	12.3%
66	Sicca Syndrome	12.1%
67	Sjogren's Syndrome	12.1%
68	Menkes Kinky Hair Syndrome	11.9%
69	Gout	11.8%
70	Pectus excavatum	11.7%
71	Cytochrome-c Oxidase Deficiency	11.6%
72	Arthritis	11.5%
73	Polyarthritis	11.5%
74	Platybasia	11.4%
75	Adrenoleukodystrophy	11.1%
76	Glycogen storage disease type II	11%
77	Multiple Epiphyseal Dysplasia	11%
78	Osteochondrodysplasias	11%
79	Hepatolenticular Degeneration	11%
80	Homocystinuria	10.7%
81	Zellweger Syndrome	10.6%
82	Refsum Disease	10.6%
83	Hyperhomocysteinemia	10.5%
84	Klippel-Feil Syndrome	10.5%
85	Synostosis	10.5%
86	Carbamoyl-Phosphate Synthase I Deficiency Disease	10.3%
87	Hypolipoproteinemias	10.3%
88	Lactose Intolerance	10.3%
89	Dwarfism	9.9%
90	Werner Syndrome	9.9%
91	Albinism	9.8%
92	Alkaptonuria	9.7%
93	Glycogen Storage Disease	9.7%
94	Hypophosphatasia	9.7%
95	Propionic acidemia	9.7%
96	Cystinosis	9.7%
97	Mitochondrial Myopathies	9.7%
98	Hyperlipidemia, Familial Combined	9.7%
99	Muscular Dystrophy	9.6%
100	Cockayne Syndrome	9.5%
101	Talipes	9.4%
102	Hyperlipoproteinemia Type III	9.3%
103	Rickets	9.3%
104	Ichthyosis, X-Linked	9.3%
105	Amyloid Neuropathies, Familial	9.3%
106	Craniosynostosis	9.2%
107	Syndactyly	9.2%
108	Brachycephaly	9.2%
109	Hip Dislocation	9.1%
110	Shoulder Dislocation	9.1%
111	Hip Dysplasia	9.1%
112	Mucopolysaccharidosis II	9.1%
113	Hyperlipoproteinemia Type IV	9.1%
114	Hyperlipoproteinemia Type V	9.1%
115	Mucopolysaccharidosis III	9%
116	Acrocephalosyndactylia	8.9%
117	Bone Diseases, Developmental	8.7%
118	Hyperostosis	8.7%
119	Myofascial Pain Syndromes	8.7%
120	Osteitis	8.7%
121	Osteitis Deformans	8.7%
122	Osteochondrosis	8.7%
123	Rhabdomyolysis	8.7%
124	Spinal Diseases	8.7%
125	Rheumatism	8.7%
126	Limb Deformities, Congenital	8.7%
127	Craniofacial Abnormalities	8.7%
128	Myotonic Dystrophy	8.7%
129	Familial Hypophosphatemic Rickets	8.6%
130	Hypokalemic periodic paralysis	8.6%
131	Wasting Syndrome	8.5%
132	Rubinstein-Taybi Syndrome	8.4%
133	Neuronal Ceroid-Lipofuscinoses	8.4%
134	Osteogenesis Imperfecta	8.4%
135	Gaucher Disease	8.3%
136	Fabry Disease	8.3%
137	Renal tubular acidosis	8.2%
138	Gigantism	8.2%
139	Spinal Neoplasms	8.2%
140	Spondylitis	8.2%
141	MELAS Syndrome	8.1%
142	Osteoporosis	8.1%
143	Bone Demineralization, Pathologic	8.1%
144	Post-Traumatic Osteoporosis	8.1%
145	Congenital Hypothyroidism	8.1%
146	Muscular Dystrophy, Duchenne	7.9%
147	Shoulder Pain	7.9%
148	Arthritis, Gouty	7.7%
149	Bone Diseases, Endocrine	7.7%
150	Jaw Abnormalities	7.6%
151	Marfan Syndrome	7.6%
152	Bone Diseases, Infectious	7.6%
153	Bone neoplasms	7.6%
154	Compartment syndromes	7.6%
155	Maxillary Diseases	7.6%
156	Tendinitis	7.6%
157	Tendinopathy	7.6%
158	Gastroschisis	7.6%
159	Renal Aminoacidurias	7.5%
160	Fanconi Syndrome	7.5%
161	Pseudohypoaldosteronism	7.5%
162	Liddle Syndrome	7.5%
163	Bone Resorption	7.5%
164	Myositis	7.5%
165	Tietze's Syndrome	7.5%
166	Isaacs syndrome	7.5%
167	Aseptic Necrosis of Bone	7.5%
168	Myotonic Disorders	7.5%
169	Craniofacial Dysostosis	7.5%
170	Acid-Base Imbalance	7.4%
171	Calcium Metabolism Disorders	7.4%
172	Iron Metabolism Disorders	7.4%
173	Phosphorus Metabolism Disorders	7.4%
174	Water-Electrolyte Imbalance	7.4%
175	Lipid Metabolism Disorders	7.4%
176	Mitochondrial Diseases	7.4%
177	Glucose Metabolism Disorders	7.4%
178	Mitochondrial Encephalomyopathies	7.1%
179	Hypercalcemia	7%
180	Hypocalcemia	7%
181	Milk-Alkali Syndrome	7%
182	Holoprosencephaly	6.9%
183	Sjogren-Larsson Syndrome	6.9%
184	Congenital clubfoot	6.9%
185	Vertical Talus	6.9%
186	Glycosuria, Renal	6.8%
187	Hypoalphalipoproteinemias	6.8%
188	Prognathism	6.8%
189	Cystic Fibrosis	6.7%
190	Poland Syndrome	6.7%
191	Medial Tibial Stress Syndrome	6.6%
192	CHARGE Syndrome	6.6%
193	Muscle Cramp	6.6%
194	Eosinophilia-Myalgia Syndrome	6.6%
195	Neoplastic Syndromes, Hereditary	6.5%
196	Muscle Rigidity	6.5%
197	Muscle Spasticity	6.5%
198	Cogwheel Rigidity	6.5%
199	Nuchal Rigidity	6.5%
200	Glycogen Storage Disease Type I	6.4%
201	Glycogen Storage Disease Type V	6.4%
202	Niemann-Pick Disease, Type C	6.4%
203	Myotonia Congenita	6.3%
204	Brain Diseases, Metabolic	6.3%
205	Pelger-Huet Anomaly	6.3%
206	Myasthenic Syndromes, Congenital	6.3%
207	Aicardi's syndrome	6.3%
208	Basal Cell Nevus Syndrome	6.3%
209	Laryngomalacia	6.2%
210	Tay-Sachs Disease	6.1%
211	Lipodystrophy	6.1%
212	Canavan Disease	6.1%
213	Alexander Disease	6.1%
214	Chronic Fatigue Syndrome	6%
215	Osteomalacia	5.9%
216	Giant Cell Epulis	5.9%
217	Muscle Weakness	5.9%
218	Welander Distal Myopathy	5.9%
219	Musculoskeletal Pain	5.8%
220	Ataxia Telangiectasia	5.8%
221	Discitis	5.6%
222	Arthropathy	5.6%
223	Porphyrias, Hepatic	5.5%
224	Anemia, Sickle Cell	5.4%
225	Thalassemia	5.4%
226	Ainhum	5.4%
227	Bunion	5.4%
228	Dysostoses	5.4%
229	Fibrodysplasia Ossificans Progressiva	5.4%
230	Myoglobinuria	5.4%
231	Myositis Ossificans	5.4%
232	Spinal Stenosis	5.4%
233	Spondylosis	5.4%
234	Tenosynovitis	5.4%
235	Intervertebral Disc Degeneration	5.4%
236	Fanconi Anemia	5.4%
237	Amelia	5.3%
238	Arachnodactyly	5.3%
239	Ectromelia	5.3%
240	Hemimelia	5.3%
241	Phocomelia	5.3%
242	Sirenomelia	5.3%
243	Polydactyly	5.3%
244	Brachydactyly	5.3%
245	Plagiocephaly	5.3%
246	Lower Extremity Deformities, Congenital	5.3%
247	Upper Extremity Deformities, Congenital	5.3%
248	Osteoporosis, Postmenopausal	5.3%
249	Eosinophilic Granuloma	5.2%
250	Myalgia	5.2%
251	Maxillofacial Abnormalities	5.1%
252	Beckwith-Wiedemann Syndrome	5.1%
253	Wolf-Hirschhorn Syndrome	5.1%
254	Micrognathism	5.1%
255	Pierre Robin Syndrome	5.1%
256	Tuberculosis, Spinal	5%
257	Autoimmune Lymphoproliferative Syndrome	5%
258	Cystinuria	5%
259	Congenital Hyperinsulinism	4.9%
260	Angioedemas, Hereditary	4.9%
261	Mandibulofacial Dysostosis	4.8%
262	Fragile X Syndrome	4.8%
263	Deformity	4.7%
264	Nutrition Disorders	4.7%
265	Kartagener Syndrome	4.7%
266	Retrognathia	4.7%
267	Anterior Compartment Syndrome	4.7%
268	Bloom Syndrome	4.7%
269	Osteomyelitis	4.7%
270	Periostitis	4.7%
271	Enthesopathy	4.7%
272	Abdominal Compartment Syndrome	4.7%
273	Alveolar Bone Loss	4.6%
274	Femur Head Necrosis	4.6%
275	Polymyositis	4.6%
276	Osteolysis	4.6%
277	Smith-Magenis syndrome	4.6%
278	Palatal Neoplasms	4.6%
279	Prader-Willi Syndrome	4.6%
280	Cri-du-Chat Syndrome	4.5%
281	Down Syndrome	4.5%
282	Trisomy 21	4.5%
283	Alstrom Syndrome	4.5%
284	Microcephaly	4.5%
285	Macrocephaly	4.5%
286	Renal Osteodystrophy	4.5%
287	Renal rickets	4.5%
288	Optic Atrophy, Hereditary, Leber	4.5%
289	Xeroderma Pigmentosum	4.5%
290	Wiskott-Aldrich Syndrome	4.4%
291	Goldenhar Syndrome	4.4%
292	Cleft Palate	4.3%
293	Kallmann Syndrome	4.3%
294	Bronchomalacia	4.2%
295	Tracheomalacia	4.2%
296	Fetal Diseases	4.1%
297	Ectodermal Dysplasia	4.1%
298	Aplasia Cutis Congenita	4.1%
299	Orbital Myositis	4.1%
300	Dupuytren Contracture	4.1%
301	Pyomyositis	4.1%
302	Acidosis	4.1%
303	Alkalosis	4.1%
304	Amyloidosis	4.1%
305	Calcinosis	4.1%
306	Hyperglycemia	4.1%
307	Hyperinsulinism	4.1%
308	Hyperkalemia	4.1%
309	Hypernatremia	4.1%
310	Hypoglycemia	4.1%
311	Hypokalemia	4.1%
312	Hyponatremia	4.1%
313	Familial Mediterranean Fever	4.1%
314	Xanthomatosis	4.1%
315	Hypophosphatemia	4.1%
316	Metabolic acidosis	4.1%
317	Dyslipidemias	4.1%
318	Iron Overload	4.1%
319	Xanthoma	4.1%
320	Acromegaly	4.1%
321	Joint Tuberculosis	4.1%
322	Tuberculosis, Osteoarticular	4.1%
323	Bone Tuberculosis	4.1%
324	Noonan Syndrome	3.9%
325	Friedreich Ataxia	3.9%
326	Tuberous Sclerosis	3.8%
327	Chondrodysplasia Punctata	3.8%
328	Enchondromatosis	3.8%
329	Lordosis	3.8%
330	Osteosclerosis	3.8%
331	Spondylolysis	3.8%
332	kyphosis	3.8%
333	Kashin-Beck Disease	3.8%
334	Kearns-Sayre syndrome	3.8%
335	Rett Syndrome	3.6%
336	Polycystic Kidney Diseases	3.6%
337	Williams Syndrome	3.6%
338	Diabetes Mellitus	3.6%
339	Dehydration	3.5%
340	Lipomatosis	3.5%
341	Water Intoxication	3.5%
342	Achlorhydria	3.5%
343	Celiac Disease	3.5%
344	Sprue, Tropical	3.5%
345	Steatorrhea	3.5%
346	Sprue	3.5%
347	Primary Ciliary Dyskinesia	3.4%
348	Retinal Dysplasia	3.3%
349	Aniridia	3.3%
350	Epidermolysis Bullosa	3.3%
351	HIV Wasting Syndrome	3.3%
352	Variegate Porphyria	3.2%
353	Acute intermittent porphyria	3.2%
354	Porphyria Cutanea Tarda	3.2%
355	Sickle Cell Trait	3.2%
356	Porencephaly	3.2%
357	Cutis Laxa	3.1%
358	Retinitis Pigmentosa	3.1%
359	Myelinolysis, Central Pontine	3.1%
360	Pigmentary retinopathy	3.1%
361	Porokeratosis	3.1%
362	Keratoderma, Palmoplantar	3.1%
363	Nesidioblastosis	3.1%
364	Glycosuria	3%
365	Chronic granulomatous disease	3%
366	Reye Syndrome	3%
367	Hepatic Encephalopathy	3%
368	Diabetic Ketoacidosis	3%
369	Meconium Aspiration Syndrome	3%
370	Kernicterus	3%
371	Melorheostosis	2.9%
372	Osteopetrosis	2.9%
373	Spondylolisthesis	2.9%
374	Mastoiditis	2.8%
375	Petrositis	2.8%
376	Duane Retraction Syndrome	2.8%
377	Pseudoxanthoma Elasticum	2.7%
378	Peutz-Jeghers Syndrome	2.7%
379	Thrombasthenia	2.7%
380	Antithrombin III Deficiency	2.7%
381	Necrobiosis Lipoidica Diabeticorum	2.7%
382	Protein C Deficiency	2.7%
383	Afibrinogenemia	2.7%
384	Dystonia Musculorum Deformans	2.7%
385	Factor VII Deficiency	2.7%
386	Factor X Deficiency	2.7%
387	Factor XII Deficiency	2.7%
388	Hemophilia A	2.7%
389	Activated Protein C Resistance	2.7%
390	Factor II deficiency	2.7%
391	Factor VIII Deficiency	2.7%
392	Factor V deficiency	2.7%
393	Factor XI Deficiency	2.7%
394	Hypoprothrombinemias	2.7%
395	Lafora Disease	2.7%
396	Unverricht-Lundborg Syndrome	2.7%
397	Anemia, Diamond-Blackfan	2.7%
398	Acute Chest Syndrome	2.7%
399	HIV-Associated Lipodystrophy Syndrome	2.6%
400	Wernicke Encephalopathy	2.6%
401	Xeroderma	2.6%
402	Mobius Syndrome	2.6%
403	Dermatomyositis	2.6%
404	Multiple Endocrine Neoplasia	2.5%
405	Abdominal Cramps	2.5%
406	Abnormalities, Drug-Induced	2.5%
407	Amniotic Band Syndrome	2.5%
408	Asphyxia Neonatorum	2.5%
409	Child Nutrition Disorders	2.5%
410	Dermatitis, Atopic	2.5%
411	Hypervitaminosis A	2.5%
412	Infant Nutrition Disorders	2.5%
413	Infant, Premature, Diseases	2.5%
414	Situs Inversus	2.5%
415	Malnutrition	2.5%
416	Infantile Colic	2.5%
417	Acidosis, Lactic	2.4%
418	Calciphylaxis	2.4%
419	Hemosiderosis	2.4%
420	Ketosis	2.4%
421	Ketonuria	2.4%
422	Ketoacidosis	2.4%
423	Ketonemia	2.4%
424	Vascular calcification	2.4%
425	Behcet Syndrome	2.2%
426	Eye Abnormalities	2.2%
427	Cardiovascular Abnormalities	2.2%
428	Polycystic Kidney, Autosomal Dominant	2.1%
429	Skin Abnormalities	2.1%
430	Lymphatic Abnormalities	2.1%
431	Congenital Microtia	2.1%
432	Anemia, Neonatal	2.1%
433	Persistent Fetal Circulation Syndrome	2.1%
434	Congenital diaphragmatic hernia	2.1%
435	Umbilical hernia	2.1%
436	Acidosis, Respiratory	2.1%
437	Adiposis Dolorosa	2.1%
438	Alkalosis, Respiratory	2.1%
439	Insulin Resistance	2.1%
440	Hyperkeratosis, Epidermolytic	2%
441	Huntington Disease	2%
442	Classical Lissencephalies and Subcortical Band Heterotopias	2%
443	Nose Neoplasms	1.9%
444	Charcot-Marie-Tooth Disease	1.9%
445	Urogenital Abnormalities	1.9%
446	Neonatal Abstinence Syndrome	1.9%
447	Nephroblastoma	1.9%
448	Gestational Diabetes	1.9%
449	Latent Autoimmune Diabetes in Adults	1.9%
450	Fetal Growth Retardation	1.9%
451	Diabetes Mellitus, Experimental	1.8%
452	Fetal Hypoxia	1.8%
453	Congenital nystagmus	1.8%
454	Fetal Alcohol Spectrum Disorders	1.8%
455	Toxoplasmosis, Congenital	1.8%
456	Syphilis, Congenital	1.8%
457	Nephrocalcinosis	1.8%
458	Tetany	1.8%
459	Papillon-Lefevre Disease	1.8%
460	Cerebral Amyloid Angiopathy	1.8%
461	Radicular Cyst	1.8%
462	Adenomatous Polyposis Coli	1.7%
463	Chorioamnionitis	1.6%
464	Primary amyloidosis	1.6%
465	Anencephaly	1.6%
466	Hypercholesterolemia	1.6%
467	Hyperlipoproteinemias	1.6%
468	Hypertriglyceridemia	1.6%
469	Hydrops Fetalis	1.5%
470	Abnormalities, Radiation-Induced	1.5%
471	Amyotrophic Lateral Sclerosis	1.5%
472	Multiple Endocrine Neoplasia Type 1	1.5%
473	Dural Arteriovenous Fistula	1.5%
474	Dextrocardia	1.4%
475	Deficiency Diseases	1.4%
476	Prune Belly Syndrome	1.4%
477	Starvation	1.4%
478	Twins, Conjoined	1.4%
479	Refeeding Syndrome	1.4%
480	Waardenburg Syndrome	1.4%
481	Turner Syndrome	1.3%
482	Klinefelter Syndrome	1.3%
483	Ophthalmia Neonatorum	1.3%
484	CREST Syndrome	1.3%
485	Scimitar Syndrome	1.2%
486	Anophthalmos	1.2%
487	Anus, Imperforate	1.2%
488	Hydranencephaly	1.2%
489	Microphthalmos	1.2%
490	Neural Tube Defects	1.2%
491	Paralysis, Obstetric	1.2%
492	Retinopathy of Prematurity	1.2%
493	Tethered Cord Syndrome	1.2%
494	Iniencephaly	1.2%
495	Craniorachischisis	1.2%
496	Exencephaly	1.2%
497	Septo-Optic Dysplasia	1.2%
498	Cortical Dysplasia	1.2%
499	Malformations of Cortical Development	1.2%
500	Anorectal Malformations	1.2%
501	Bronchopulmonary Dysplasia	1.2%
502	Frontotemporal dementia	1.1%
503	Blepharophimosis	1%
504	Laryngostenosis	1%
505	Mouth Abnormalities	1%
506	Respiratory Distress Syndrome, Newborn	1%
507	Denys-Drash Syndrome	1%
508	Esophageal Atresia	1%
509	Intestinal Atresia	1%
510	Horseshoe Kidney	1%
511	Acrodermatitis	1%
512	Lymphangiectasis, Intestinal	1%
513	Gianotti-Crosti Syndrome	1%
514	Choanal Atresia	0.9%
515	Tracheobronchomegaly	0.9%
516	Laryngocele	0.9%
517	Choledochal Cyst	0.9%
518	Hermaphroditism	0.9%
519	Disorders of Sex Development	0.9%
520	Cryptorchidism	0.9%
521	Hypospadias	0.9%
522	Central Nervous System Cysts	0.9%
523	Dandy-Walker Syndrome	0.9%
524	Leukomalacia, Periventricular	0.9%
525	POEMS Syndrome	0.9%
526	Obesity	0.9%
527	Bladder Exstrophy	0.8%
528	Epispadias	0.8%
529	Multicystic Dysplastic Kidney	0.8%
530	Kwashiorkor	0.8%
531	Magnesium Deficiency	0.8%
532	Potassium Deficiency	0.8%
533	Protein Deficiency	0.8%
534	Avitaminosis	0.8%
535	Ectopia Cordis	0.7%
536	Meningomyelocele	0.7%
537	Spina Bifida	0.7%
538	Single umbilical artery	0.7%
539	Aortic coarctation	0.6%
540	Cor Triatriatum	0.6%
541	Coronary Vessel Anomalies	0.6%
542	Dental Enamel Hypoplasia	0.6%
543	Patent ductus arteriosus	0.6%
544	Ebstein Anomaly	0.6%
545	Heart Septal Defects	0.6%
546	Hyaline Membrane Disease	0.6%
547	Hypodontia	0.6%
548	Macrostomia	0.6%
549	Meningocele	0.6%
550	Microstomia	0.6%
551	Tetralogy of Fallot	0.6%
552	Transposition of Great Vessels	0.6%
553	Hypoplastic Left Heart Syndrome	0.6%
554	May-Thurner Syndrome	0.6%
555	Encephalocele	0.6%
556	Wolff-Parkinson-White Syndrome	0.6%
557	Obesity, Abdominal	0.6%
558	Long QT Syndrome	0.5%
559	Tricuspid Atresia	0.5%
560	Arrhythmogenic Right Ventricular Dysplasia	0.5%
561	Gonadal Dysgenesis	0.5%
562	Adrenogenital Syndrome	0.5%
563	Ovotesticular Disorders of Sex Development	0.5%
564	Ascorbic Acid Deficiency	0.5%
565	Vitamin A Deficiency	0.5%
566	Vitamin D Deficiency	0.5%
567	Vitamin E Deficiency	0.5%
568	Marasmus	0.5%
569	Pediatric Obesity	0.5%
570	Hyperandrogenism	0.5%
571	Dermal Sinus	0.5%
572	Spina Bifida Cystica	0.5%
573	Spina Bifida Occulta	0.5%
574	Lissencephaly	0.5%
575	Polymicrogyria	0.5%
576	Pachygyria	0.5%
577	Schizencephaly	0.5%
578	Periventricular Nodular Heterotopia	0.5%
579	Vitamin K Deficiency	0.4%
580	Aortopulmonary Septal Defect	0.4%
581	Double Outlet Right Ventricle	0.4%
582	Endocardial Cushion Defects	0.4%
583	Myocardial bridging	0.4%
584	Aorticopulmonary Septal Defect	0.4%
585	Folic Acid Deficiency	0.4%
586	Pellagra	0.4%
587	Thiamine Deficiency	0.4%
588	Vitamin B 12 Deficiency	0.4%
589	Vitamin B 6 Deficiency	0.4%
590	Pyridoxine Deficiency	0.4%
591	Romano-Ward Syndrome	0.4%
592	Beriberi	0.3%
593	Scurvy	0.3%
594	Truncus Arteriosus, Persistent	0.3%
595	Arteriovenous fistula	0.3%
596	Anemia, Pernicious	0.3%
597	Subacute Combined Degeneration	0.2%

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