SLE
MCID: LPS004
MIFTS: 61

Lupus Erythematosus (SLE)

Categories: Blood diseases, Bone diseases, Genetic diseases, Immune diseases, Nephrological diseases, Rare diseases, Skin diseases

Aliases & Classifications for Lupus Erythematosus

MalaCards integrated aliases for Lupus Erythematosus:

Name: Lupus Erythematosus 12 74 52 54 15 71 32
Lupus 12 52 15
Subacute Cutaneous Lupus 52 71
Disseminated Lupus Erythematosus 52
Lupus Erythematosus, Systemic 71
Systemic Lupus Erythematosus 52
Lupus Erythematosus, Discoid 71
Lupus Vulgaris 71
Discoid Lupus 52
Sle 52

Classifications:



External Ids:

Disease Ontology 12 DOID:8857
ICD9CM 34 695.4
NCIt 49 C27153
SNOMED-CT 67 200936003
ICD10 32 L93
UMLS 71 C0024131 C0024138 C0024141 more

Summaries for Lupus Erythematosus

NIH Rare Diseases : 52 Lupus is an autoimmune disease that can affect almost every organ in the body. Symptoms of lupus can range from very mild to life-threatening. There are three main types of lupus; systemic lupus erythematosus , discoid lupus , and drug-induced lupus. Symptoms may include pain or swelling in joints, muscle pain, fever, red rashes, most often on the face (also called the "butterfly rash"), hair loss, chest pain, sensitivity to the sun, swelling in legs or around the eyes, and feeling tired. Genetics is thought to play a role in the development of lupus along with other lifestyle and environmental factors . Studies suggest that a number of different genes may be involved in determining a person's likelihood of developing the disease, which tissues and organs are affected, and the severity of disease. Lupus is more common in young women. The treatment of lupus depends on the severity of the condition and what parts of the body are affected. Treatment may include acetaminophen , ibuprofen , antimalarial drugs, anti-inflammatory steroids, immunosuppressive drugs, and other such as BLyS-specific inhibitors (Belimumab ).

MalaCards based summary : Lupus Erythematosus, also known as lupus, is related to systemic lupus erythematosus 16 and cutaneous lupus erythematosus, and has symptoms including rashes, seizures and pruritus. An important gene associated with Lupus Erythematosus is TLR5 (Toll Like Receptor 5), and among its related pathways/superpathways are Innate Immune System and Toll-like Receptor Signaling Pathway. The drugs tannic acid and Benzocaine have been mentioned in the context of this disorder. Affiliated tissues include t cells, b cells and skin, and related phenotypes are Decreased viability and Decreased viability

Disease Ontology : 12 An autoimmune hypersensitivity disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs, and has material basis in autoimmune disorder.

Wikipedia : 74 Lupus erythematosus is a collection of autoimmune diseases in which the human immune system becomes... more...

Related Diseases for Lupus Erythematosus

Diseases in the Lupus Erythematosus family:

Systemic Lupus Erythematosus Systemic Lupus Erythematosus 15
Systemic Lupus Erythematosus 1 Systemic Lupus Erythematosus 2
Systemic Lupus Erythematosus 3 Systemic Lupus Erythematosus 4
Systemic Lupus Erythematosus 5 Systemic Lupus Erythematosus 6
Systemic Lupus Erythematosus 7 Systemic Lupus Erythematosus 8
Systemic Lupus Erythematosus 9 Systemic Lupus Erythematosus 10
Systemic Lupus Erythematosus 11 Systemic Lupus Erythematosus 12
Systemic Lupus Erythematosus 13 Systemic Lupus Erythematosus 14
Systemic Lupus Erythematosus 16

Diseases related to Lupus Erythematosus via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 2323, show less)
# Related Disease Score Top Affiliating Genes
1 systemic lupus erythematosus 16 35.5 DNASE1L3 DNASE1 C4A C1QA
2 cutaneous lupus erythematosus 35.5 TRIM21 IRF5 CTLA4
3 neonatal lupus erythematosus 35.4 TRIM21 C4A
4 subacute cutaneous lupus erythematosus 35.2 TRIM21 C1QA
5 systemic lupus erythematosus 35.1 TRIM21 TNFSF4 TLR5 STAT4 SSB SNRPB
6 pediatric systemic lupus erythematosus 35.0 STAT4 C4B C4A
7 vitiligo-associated multiple autoimmune disease susceptibility 1 34.6 PTPN22 PDCD1 CTLA4 C4B
8 c1q deficiency 33.9 C1QC C1QB C1QA
9 sjogren syndrome 33.7 TRIM21 TNFSF4 SSB
10 aicardi-goutieres syndrome 33.6 TLR5 IRF5 DNASE1L3
11 complement factor i deficiency 33.0 C4B C4A
12 autoimmune disease 32.9 TRIM21 STAT4 PTPN22 PDCD1 IRF5 FCGR2B
13 systemic scleroderma 32.9 TRIM21 STAT4 IRF5
14 exanthem 32.7 TRIM21 PDCD1 CTLA4
15 glomerulonephritis 32.6 C4B C4A C1QC C1QB C1QA
16 thrombocytopenia 32.5 TLR5 PTPN22 PDCD1 FCGR2B CTLA4
17 rheumatoid arthritis 32.3 STAT4 PTPN22 PDCD1 IRF5 FCGR2B CTLA4
18 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 32.2 PTPN22 CTLA4
19 heart block, congenital 31.8 TRIM21 SSB
20 primary biliary cirrhosis 31.7 TLR5 STAT4 PTPN22 PDCD1 IRF5 CTLA4
21 celiac disease 1 31.6 TLR5 STAT4 SNRPB PTPN22 CTLA4
22 mononeuritis multiplex 31.4 TRIM21 SSB
23 common variable immunodeficiency 31.4 TNFSF4 FCGR2B CTLA4 CR2
24 diabetes mellitus, type i 31.2 TLR5 PTPN22 PDCD1 CTLA4 C4A
25 diffuse scleroderma 31.1 TRIM21 BANK1
26 parotitis 31.0 TRIM21 SSB
27 second-degree atrioventricular block 30.9 TRIM21 SSB
28 limited scleroderma 30.9 TRIM21 SSB IRF5 BANK1
29 xerophthalmia 30.9 TRIM21 SSB
30 behcet syndrome 30.8 TLR5 STAT4 PTPN22 CTLA4 C4A
31 polyclonal hypergammaglobulinemia 30.7 TRIM21 SSB
32 multifocal motor neuropathy 30.6 PTPN22 FCGR2B BANK1
33 complement component 3 deficiency 30.6 C4B C4A
34 bone inflammation disease 30.5 TLR5 PTPN22 CTLA4
35 parotid disease 30.5 TRIM21 SSB
36 complement component 5 deficiency 30.3 C4B C4A
37 third-degree atrioventricular block 30.1 TRIM21 SSB
38 oligoarticular juvenile idiopathic arthritis 30.0 STAT4 PTPN22
39 lupus erythematosus tumidus 13.0
40 discoid lupus erythematosus 13.0
41 drug-induced lupus erythematosus 12.9
42 systemic lupus erythematosus 1 12.9
43 systemic lupus erythematosus 2 12.8
44 systemic lupus erythematosus 10 12.8
45 systemic lupus erythematosus 9 12.8
46 systemic lupus erythematosus 6 12.8
47 systemic lupus erythematosus 11 12.8
48 lupus erythematosus panniculitis 12.7
49 chronic cutaneous lupus erythematosus 12.6
50 systemic lupus erythematosus with hemolytic anemia 1 12.6
51 neonatal systemic lupus erythematosus 12.6
52 systemic lupus erythematosus 3 12.6
53 systemic lupus erythematosus 4 12.6
54 systemic lupus erythematosus 7 12.6
55 systemic lupus erythematosus 8 12.6
56 systemic lupus erythematosus 15 12.6
57 systemic lupus erythematosus 13 12.6
58 systemic lupus erythematosus 5 12.6
59 systemic lupus erythematosus 12 12.6
60 systemic lupus erythematosus 14 12.6
61 chilblain lupus 1 12.6
62 systemic lupus erythematosus with nephritis 1 12.6
63 systemic lupus erythematosus with nephritis 2 12.6
64 systemic lupus erythematosus with nephritis 3 12.6
65 rare cutaneous lupus erythematosus 12.5
66 hypertrophic or verrucous lupus erythematosus 12.5
67 discoid lupus erythematosus of eyelid 12.4
68 idiopathic non-lupus full-house nephropathy 12.2
69 mixed connective tissue disease 12.0
70 antiphospholipid syndrome 12.0
71 complement component 2 deficiency 11.8
72 spondyloenchondrodysplasia with immune dysregulation 11.8
73 raynaud phenomenon 11.8
74 anemia, autoimmune hemolytic 11.7
75 fibromyalgia 11.7
76 macrophage activation syndrome 11.7
77 pure red-cell aplasia 11.7
78 neuromyelitis optica 11.7
79 progressive multifocal leukoencephalopathy 11.7
80 hypogonadotropic hypogonadism 11.7
81 retinal vasculitis 11.7
82 undifferentiated connective tissue disease 11.7
83 epidermolysis bullosa acquisita 11.7
84 rapidly progressive glomerulonephritis 11.7
85 t-cell lymphoma, subcutaneous panniculitis-like 11.7
86 distal renal tubular acidosis 11.7
87 pemphigus erythematosus 11.7
88 jaccoud's syndrome 11.7
89 raynaud disease 11.7
90 complement component 3 deficiency, autosomal recessive 11.7
91 spondyloenchondrodysplasia 11.6
92 complement component c1s deficiency 11.6
93 sneddon syndrome 11.6
94 glomerulopathy with fibronectin deposits 2 11.6
95 pseudopelade of brocq 11.6
96 chilblain lupus 2 11.5
97 pseudo-torch syndrome 1 11.3
98 autoimmune disease 6 11.3
99 acquired pure red cell aplasia 11.3
100 autoimmune inner ear disease 11.3
101 c1q nephropathy 11.3
102 insulin-resistance type b 11.3
103 singleton-merten syndrome 11.3
104 lupus - neurological sequelae 11.3
105 vasculitis 11.2
106 connective tissue disease 11.1
107 idiopathic cd4-positive t-lymphocytopenia 11.0
108 thymus cancer 11.0
109 pili torti 11.0
110 neutropenia 11.0
111 purpura 11.0
112 hemolytic anemia 10.9
113 scleroderma, familial progressive 10.9
114 alopecia 10.9
115 pericarditis 10.9
116 lymphopenia 10.9
117 nephrotic syndrome 10.9
118 dermatomyositis 10.9
119 systemic autoimmune disease 10.9
120 enthesopathy 10.9
121 pulmonary hypertension 10.9
122 skin disease 10.8
123 atherosclerosis susceptibility 10.8
124 thrombophilia due to thrombin defect 10.8
125 vascular disease 10.8
126 pre-eclampsia 10.8
127 panniculitis 10.8
128 end stage renal disease 10.8
129 pancytopenia 10.8
130 myelitis 10.8
131 hemopericardium 10.8
132 pericardial effusion 10.8
133 endocarditis 10.8
134 neuropathy 10.8
135 osteonecrosis 10.8
136 thrombotic thrombocytopenic purpura 10.8
137 myocarditis 10.8
138 thrombosis 10.8
139 transverse myelitis 10.8
140 lichen planus 10.8
141 proliferative glomerulonephritis 10.7
142 myasthenia gravis 10.7
143 collagen disease 10.7
144 myositis 10.7
145 peripheral nervous system disease 10.7
146 lung disease 10.7
147 rheumatoid factor-negative polyarticular juvenile idiopathic arthritis 10.7 STAT4 PTPN22
148 type 1 diabetes mellitus 12 10.7 PTPN22 CTLA4
149 juvenile dermatitis herpetiformis 10.7 C4B C4A
150 autoimmune disease of skin and connective tissue 10.7 PTPN22 PDCD1 CTLA4
151 thyroiditis 10.7
152 cytokine deficiency 10.7
153 arthritis 10.7
154 psoriasis 10.7
155 diffuse cutaneous systemic sclerosis 10.7 STAT4 IRF5 BANK1
156 avascular necrosis 10.7
157 kidney disease 10.7
158 pustulosis of palm and sole 10.7
159 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 10.7
160 tick-borne relapsing fever 10.7 C4B C4A
161 deficiency anemia 10.7
162 rickets 10.7
163 type 1 diabetes mellitus 2 10.7 PTPN22 CTLA4
164 chorea, childhood-onset, with psychomotor retardation 10.7
165 choreatic disease 10.7
166 hypothyroidism 10.7
167 pancreatitis 10.7
168 cerebrovascular disease 10.7
169 cardiac tamponade 10.7
170 herpes zoster 10.7
171 splenomegaly 10.7
172 headache 10.7
173 interstitial lung disease 10.7
174 autoimmune cardiomyopathy 10.7 PDCD1 CTLA4
175 erythema multiforme 10.7
176 arthropathy 10.7
177 peritonitis 10.7
178 syphilis 10.7
179 diffuse infiltrative lymphocytosis syndrome 10.7 TRIM21 SSB
180 dermatitis 10.7
181 acute pancreatitis 10.7
182 mood disorder 10.7
183 meningitis 10.7
184 encephalopathy 10.7
185 nervous system disease 10.7
186 eclampsia 10.7
187 polyneuropathy 10.7
188 47,xyy 10.7
189 polymyositis 10.6
190 pulmonary hypertension, primary, 1 10.6
191 autoimmune hepatitis 10.6
192 lipid metabolism disorder 10.6
193 autoimmune disease of exocrine system 10.6 TRIM21 STAT4 SSB IRF5
194 neuritis 10.6
195 juvenile rheumatoid arthritis 10.6
196 mononeuritis of upper limb and mononeuritis multiplex 10.6 TRIM21 SSB
197 membranous nephropathy 10.6
198 protein-losing enteropathy 10.6
199 immunodeficiency due to a classical component pathway complement deficiency 10.6 C4B C4A C1QC C1QB C1QA
200 pemphigus 10.6
201 pleurisy 10.6
202 central nervous system disease 10.6
203 respiratory failure 10.6
204 esophageal tuberculosis 10.6 CTLA4 CR2
205 potocki-shaffer syndrome 10.6 TRIM21 STAT4 SSB IRF5 CR2
206 hyperprolactinemia 10.6
207 lymphadenitis 10.6
208 diffuse alveolar hemorrhage 10.6
209 cystitis 10.6
210 pulmonary embolism 10.6
211 thrombotic microangiopathy 10.6
212 plica syndrome 10.6
213 urticaria 10.6
214 synovitis 10.6
215 acute kidney failure 10.6
216 lymphoma 10.6
217 bacterial infectious disease 10.6
218 optic neuritis 10.6
219 inflammatory spondylopathy 10.6
220 spondylitis 10.6
221 bullous pemphigoid 10.6
222 aneurysm 10.6
223 congestive heart failure 10.6
224 myopathy 10.6
225 spondyloarthropathy 1 10.6
226 sarcoidosis 1 10.6
227 allergic hypersensitivity disease 10.6
228 seizure disorder 10.6
229 autoimmune disease of musculoskeletal system 10.6 TRIM21 TLR5 STAT4 SSB PTPN22 IRF5
230 aseptic meningitis 10.6
231 squamous cell carcinoma 10.6
232 thrombocytopenic purpura, autoimmune 10.6
233 thymoma, familial 10.6
234 atrioventricular block 10.6
235 thymoma 10.6
236 mitral valve insufficiency 10.6
237 porphyria 10.6
238 complement deficiency 10.6
239 diarrhea 10.5
240 osteoporosis 10.5
241 colitis 10.5
242 angioedema 10.5
243 heart valve disease 10.5
244 immune deficiency disease 10.5
245 amyloidosis 10.5
246 bone mineral density quantitative trait locus 8 10.5
247 bone mineral density quantitative trait locus 15 10.5
248 keratosis 10.5
249 lung non-squamous non-small cell carcinoma 10.5 PDCD1 CTLA4
250 pneumonia 10.5
251 tetanus 10.5
252 b-cell lymphoma 10.5
253 hashimoto thyroiditis 10.5
254 amenorrhea 10.5
255 aphthous stomatitis 10.5
256 red cell aplasia 10.5
257 migraine with or without aura 1 10.5
258 aspergillosis 10.5
259 guillain-barre syndrome 10.5
260 liver disease 10.5
261 placenta disease 10.5
262 septic arthritis 10.5
263 hypercholesterolemia, familial, 1 10.5
264 proteasome-associated autoinflammatory syndrome 1 10.5
265 juvenile arthritis 10.5
266 intestinal pseudo-obstruction 10.5
267 calcinosis 10.5
268 stevens-johnson syndrome/toxic epidermal necrolysis 10.5
269 infective endocarditis 10.5
270 heart disease 10.5
271 aortic aneurysm 10.5
272 encephalitis 10.5
273 inflammatory bowel disease 10.5
274 disseminated intravascular coagulation 10.5
275 dermatitis herpetiformis 10.5
276 crohn's disease 10.5
277 tenosynovitis 10.5
278 myelofibrosis 10.5
279 yemenite deaf-blind hypopigmentation syndrome 10.5
280 lipoprotein quantitative trait locus 10.5
281 kikuchi disease 10.5
282 dermatitis herpetiformis, familial 10.5
283 pulmonary fibrosis 10.5
284 liver cirrhosis 10.5
285 polyarteritis nodosa 10.5
286 multiple sclerosis 10.5
287 intracranial hypertension 10.5
288 depression 10.5
289 hyperlipoproteinemia, type iii 10.5
290 visual epilepsy 10.5
291 toxic shock syndrome 10.5
292 hyperthyroidism 10.5
293 cerebral atrophy 10.5
294 cytomegalovirus infection 10.5
295 neurofibromatosis, type ii 10.5
296 vitiligo-associated multiple autoimmune disease susceptibility 6 10.5
297 psoriatic arthritis 10.5
298 anxiety 10.5
299 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.5
300 cholecystitis 10.5
301 arteries, anomalies of 10.5
302 coronary heart disease 1 10.5
303 agammaglobulinemia 10.5
304 cryoglobulinemia 10.5
305 acute myocardial infarction 10.5
306 hypertriglyceridemia, familial 10.5
307 dowling-degos disease 1 10.5
308 graves' disease 10.5
309 telangiectasis 10.5
310 retinal vascular disease 10.5
311 peripheral vascular disease 10.4
312 sensorineural hearing loss 10.4
313 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 10.4
314 hydrocephalus 10.4
315 gout 10.4
316 thrombocytopenia due to platelet alloimmunization 10.4
317 bronchiolitis 10.4
318 chronic granulomatous disease 10.4
319 thrombophlebitis 10.4
320 chickenpox 10.4
321 aplastic anemia 10.4
322 angina pectoris 10.4
323 cryptococcal meningitis 10.4
324 rheumatic fever 10.4
325 hepatitis c 10.4
326 optic nerve disease 10.4
327 hepatitis 10.4
328 uremia 10.4
329 cataract 10.4
330 evans' syndrome 10.4
331 fasciitis 10.4
332 catastrophic antiphospholipid syndrome 10.4
333 ataxia and polyneuropathy, adult-onset 10.4
334 myocardial infarction 10.4
335 severe cutaneous adverse reaction 10.4
336 graft-versus-host disease 10.4
337 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 10.4
338 interstitial cystitis 10.4
339 pulmonary tuberculosis 10.4
340 ischemia 10.4
341 aortic valve insufficiency 10.4
342 ulcerative colitis 10.4
343 acute transverse myelitis 10.4
344 erythema multiforme major 10.4
345 atrial standstill 1 10.4
346 meningoencephalitis 10.4
347 uveitis 10.4
348 hepatitis b 10.4
349 acquired immunodeficiency syndrome 10.4
350 chronic kidney disease 10.4
351 localized scleroderma 10.4
352 porphyria cutanea tarda 10.4
353 lymphoma, hodgkin, classic 10.4
354 myeloma, multiple 10.4
355 keratoconjunctivitis sicca 10.4
356 epidermolysis bullosa 10.4
357 cerebritis 10.4
358 dermatophytosis 10.4
359 48,xyyy 10.4
360 immunoglobulin alpha deficiency 10.4
361 cryptococcosis 10.4
362 renal tubular acidosis 10.4
363 mitral valve stenosis 10.4
364 hypereosinophilic syndrome 10.4
365 ocular motor apraxia 10.4
366 lymphoproliferative syndrome 10.4
367 osteomyelitis 10.4
368 portal hypertension 10.4
369 keratoconjunctivitis 10.4
370 miliary tuberculosis 10.4
371 granulocytopenia 10.4
372 pfeiffer syndrome 10.4
373 annular erythema 10.4
374 triiodothyronine receptor auxiliary protein 10.4
375 intracranial hypertension, idiopathic 10.4
376 lymphoma, non-hodgkin, familial 10.4
377 bone mineral density quantitative trait locus 3 10.4
378 kala-azar 1 10.4
379 hepatitis c virus 10.4
380 nocardiosis 10.4
381 bronchiolitis obliterans 10.4
382 iga glomerulonephritis 10.4
383 leishmaniasis 10.4
384 diffuse large b-cell lymphoma 10.4
385 salmonellosis 10.4
386 neuroretinitis 10.4
387 acute cystitis 10.4
388 hyperparathyroidism 10.4
389 acalculous cholecystitis 10.4
390 paraplegia 10.4
391 periodontitis 10.4
392 pemphigus vulgaris, familial 10.4
393 homocysteinemia 10.4
394 hemiplegia 10.4
395 brucellosis 10.4
396 papilloma 10.4
397 retinitis 10.4
398 conjunctivitis 10.4
399 visceral leishmaniasis 10.4
400 dysphagia 10.4
401 familial mediterranean fever 10.3
402 stroke, ischemic 10.3
403 hemophagocytic lymphohistiocytosis 10.3
404 ischemic colitis 10.3
405 aortic dissection 10.3
406 mononeuropathy 10.3
407 pyuria 10.3
408 hereditary angioedema 10.3
409 transient cerebral ischemia 10.3
410 cellulitis 10.3
411 measles 10.3
412 autonomic dysfunction 10.3
413 complement component 4a deficiency 10.3
414 invasive aspergillosis 10.3
415 constrictive pericarditis 10.3
416 branch retinal artery occlusion 10.3
417 membranoproliferative glomerulonephritis 10.3
418 rhinitis 10.3
419 ileus 10.3
420 retinal artery occlusion 10.3
421 alopecia areata 10.3
422 hypoglycemia 10.3
423 anca-associated vasculitis 10.3
424 hansen's disease 10.3
425 rapidly involuting congenital hemangioma 10.3
426 glomerular disease 10.3
427 retinal detachment 10.3
428 leprosy 3 10.3
429 body mass index quantitative trait locus 1 10.3
430 mycobacterium tuberculosis 1 10.3
431 interstitial nephritis 10.3
432 candidiasis 10.3
433 thrombophilia 10.3
434 pyoderma 10.3
435 thyroid gland disease 10.3
436 demyelinating polyneuropathy 10.3
437 herpes simplex 10.3
438 back pain 10.3
439 fibrosis of extraocular muscles, congenital, 1 10.3
440 dermatitis, atopic 10.3
441 allergic rhinitis 10.3
442 covid-19 10.3
443 leukemia 10.3
444 dilated cardiomyopathy 10.3
445 cholestasis 10.3
446 squamous cell papilloma 10.3
447 pneumothorax 10.3
448 retinal vein occlusion 10.3
449 skin carcinoma 10.3
450 pyoderma gangrenosum 10.3
451 subacute delirium 10.3
452 pathologic nystagmus 10.3
453 hemophilia 10.3
454 acquired hemophilia 10.3
455 leukemia, chronic lymphocytic 10.3
456 kearns-sayre syndrome 10.3
457 granulomatosis with polyangiitis 10.3
458 central retinal artery occlusion 10.3
459 hellp syndrome 10.3
460 childhood type dermatomyositis 10.3
461 papilledema 10.3
462 epilepsy 10.3
463 polyradiculoneuropathy 10.3
464 granulomatous dermatitis 10.3
465 mucormycosis 10.3
466 rosacea 10.3
467 erythrokeratoderma ''en cocardes'' 10.3
468 tremor 10.3
469 b-cell growth factor 10.3
470 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.3
471 renal hypertension 10.3
472 autonomic neuropathy 10.3
473 focal segmental glomerulosclerosis 10.3
474 gastritis 10.3
475 mesangial proliferative glomerulonephritis 10.3
476 immune-complex glomerulonephritis 10.3
477 aortitis 10.3
478 sleep disorder 10.3
479 fatty liver disease 10.3
480 necrotizing fasciitis 10.3
481 sickle cell disease 10.3
482 leukoplakia 10.3
483 perniosis 10.3
484 cerebral aneurysms 10.3
485 pik3ca-related overgrowth syndrome 10.3
486 aortic aneurysm, familial abdominal, 1 10.3
487 thrombophilia due to activated protein c resistance 10.3
488 budd-chiari syndrome 10.3
489 autoimmune lymphoproliferative syndrome 10.3
490 malignant atrophic papulosis 10.3
491 neutrophilic dermatosis, acute febrile 10.3
492 hemorrhagic cystitis 10.3
493 drug allergy 10.3
494 bone resorption disease 10.3
495 hypoparathyroidism 10.3
496 hepatitis a 10.3
497 crescentic glomerulonephritis 10.3
498 mental depression 10.3
499 ichthyosis 10.3
500 histoplasmosis 10.3
501 constipation 10.3
502 iron metabolism disease 10.3
503 contact dermatitis 10.3
504 tricuspid valve insufficiency 10.3
505 chronic inflammatory demyelinating polyradiculoneuropathy 10.3
506 severe combined immunodeficiency 10.3
507 intestinal obstruction 10.3
508 exophthalmos 10.3
509 blepharitis 10.3
510 bacterial meningitis 10.3
511 chronic graft versus host disease 10.3
512 frontal fibrosing alopecia 10.3
513 kawasaki disease 10.2
514 ptosis 10.2
515 acquired von willebrand syndrome 10.2
516 hydronephrosis 10.2
517 cortical blindness 10.2
518 goiter 10.2
519 hemolytic-uremic syndrome 10.2
520 pleural disease 10.2
521 hypersensitivity reaction type iii disease 10.2
522 cheilitis 10.2
523 status epilepticus 10.2
524 gastroenteritis 10.2
525 arteriosclerosis 10.2
526 demyelinating disease 10.2
527 intermittent claudication 10.2
528 acute myocarditis 10.2
529 calciphylaxis 10.2
530 infertility 10.2
531 axonal neuropathy 10.2
532 scabies 10.2
533 appendicitis 10.2
534 influenza 10.2
535 stomatitis 10.2
536 toxoplasmosis 10.2
537 nodular regenerative hyperplasia 10.2
538 keratitis, hereditary 10.2
539 pernicious anemia 10.2
540 malaria 10.2
541 mucositis 10.2
542 silicosis 10.2
543 premature menopause 10.2
544 malignant hypertension 10.2
545 pneumatosis cystoides intestinalis 10.2
546 scleritis 10.2
547 viral hepatitis 10.2
548 central retinal vein occlusion 10.2
549 relapsing polychondritis 10.2
550 endometriosis 10.2
551 keratoacanthoma 10.2
552 central nervous system vasculitis 10.2
553 paralytic ileus 10.2
554 hypocomplementemic urticarial vasculitis 10.2
555 ichthyosis, acquired 10.2
556 paresthesia 10.2
557 cardiogenic shock 10.2
558 bladder cancer 10.2
559 breast cancer 10.2
560 felty syndrome 10.2
561 lichen sclerosus et atrophicus 10.2
562 temporal arteritis 10.2
563 orthostatic intolerance 10.2
564 myelodysplastic syndrome 10.2
565 gastrointestinal ulceration, recurrent, with dysfunctional platelets 10.2
566 cryptogenic organizing pneumonia 10.2
567 strongyloidiasis 10.2
568 severe pre-eclampsia 10.2
569 chronic interstitial cystitis 10.2
570 protein s deficiency 10.2
571 folliculitis 10.2
572 diffuse glomerulonephritis 10.2
573 movement disease 10.2
574 internuclear ophthalmoplegia 10.2
575 neuroblastoma 10.2
576 osteoarthritis 10.2
577 cholangitis 10.2
578 tuberculous meningitis 10.2
579 complement component 4, partial deficiency of 10.2
580 acetylation, slow 10.2
581 cervical cancer 10.2
582 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 10.2
583 joint laxity, short stature, and myopia 10.2
584 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 10.2
585 rheumatic heart disease 10.2
586 c1 inhibitor deficiency 10.2
587 aphasia 10.2
588 spondyloarthropathy 10.2
589 adult respiratory distress syndrome 10.2
590 pulmonary edema 10.2
591 myopia 10.2
592 hemosiderosis 10.2
593 hyperuricemia 10.2
594 hypogonadism 10.2
595 intestinal perforation 10.2
596 skin atrophy 10.2
597 gingivitis 10.2
598 inappropriate adh syndrome 10.2
599 hypertrichosis 10.2
600 rubella 10.2
601 intermediate coronary syndrome 10.2
602 lymphangiectasis 10.2
603 chronic pain 10.2
604 posttransplant acute limbic encephalitis 10.2
605 thyroid carcinoma 10.2
606 acanthosis nigricans 10.2
607 progressive familial heart block, type ia 10.2
608 colorectal cancer 10.2
609 cryoglobulinemia, familial mixed 10.2
610 hypertension, essential 10.2
611 noonan syndrome 1 10.2
612 porphyria, acute intermittent 10.2
613 acrocallosal syndrome 10.2
614 takayasu arteritis 10.2
615 major depressive disorder 10.2
616 alexithymia 10.2
617 diffuse alopecia areata 10.2
618 glucocorticoid-induced osteoporosis 10.2
619 cytomegalovirus retinitis 10.2
620 hepatic veno-occlusive disease 10.2
621 mastitis 10.2
622 primary hyperparathyroidism 10.2
623 neurogenic bladder 10.2
624 alcohol use disorder 10.2
625 central nervous system lymphoma 10.2
626 cranial nerve palsy 10.2
627 urinary tract obstruction 10.2
628 bronchitis 10.2
629 reactive arthritis 10.2
630 neurofibromatosis 10.2
631 actinic keratosis 10.2
632 learning disability 10.2
633 diabetes mellitus 10.2
634 iridocyclitis 10.2
635 amaurosis fugax 10.2
636 limbic encephalitis 10.2
637 oral lichen planus 10.2
638 pseudo-turner syndrome 10.2
639 sudden sensorineural hearing loss 10.2
640 secondary hemophagocytic lymphohistiocytosis 10.2
641 amyotrophic lateral sclerosis 1 10.1
642 diabetes mellitus, noninsulin-dependent 10.1
643 lymphoma, mucosa-associated lymphoid type 10.1
644 hand skill, relative 10.1
645 intussusception 10.1
646 down syndrome 10.1
647 chondrodysplasia punctata syndrome 10.1
648 mycosis fungoides 10.1
649 graves disease 1 10.1
650 sickle cell anemia 10.1
651 progressive familial heart block, type ib 10.1
652 ovarian hyperstimulation syndrome 10.1
653 human immunodeficiency virus type 1 10.1
654 cholangitis, primary sclerosing 10.1
655 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 10.1
656 peripheral artery disease 10.1
657 crohn's colitis 10.1
658 angioimmunoblastic t-cell lymphoma 10.1
659 henoch-schoenlein purpura 10.1
660 sarcoma 10.1
661 esophageal varix 10.1
662 diphtheria 10.1
663 lyme disease 10.1
664 hypertrophic cardiomyopathy 10.1
665 von willebrand's disease 10.1
666 quadriplegia 10.1
667 right bundle branch block 10.1
668 facial paralysis 10.1
669 acute poststreptococcal glomerulonephritis 10.1
670 adult-onset still's disease 10.1
671 sclerosing cholangitis 10.1
672 norwegian scabies 10.1
673 impotence 10.1
674 thrombocytosis 10.1
675 pharyngitis 10.1
676 lateral sclerosis 10.1
677 sensory peripheral neuropathy 10.1
678 splenic infarction 10.1
679 bilirubin metabolic disorder 10.1
680 histiocytosis 10.1
681 placental insufficiency 10.1
682 hyperglycemia 10.1
683 spindle cell sarcoma 10.1
684 macular retinal edema 10.1
685 hemoglobinuria 10.1
686 adenoma 10.1
687 peptic ulcer disease 10.1
688 erythromelalgia 10.1
689 scotoma 10.1
690 diabetes insipidus 10.1
691 bronchiectasis 10.1
692 amyloidosis aa 10.1
693 banti's syndrome 10.1
694 chromosomal triplication 10.1
695 linear scleroderma 10.1
696 primary central nervous system lymphoma 10.1
697 retroperitoneal fibrosis 10.1
698 reversible cerebral vasoconstriction syndrome 10.1
699 spasticity 10.1
700 pseudo-meigs syndrome 10.1
701 acute liver failure 10.1
702 inclusion body myositis 10.1
703 papillomatosis, confluent and reticulated 10.1
704 pulmonary hemosiderosis 10.1
705 varicose veins 10.1
706 vasculitis, lymphocytic, nodular 10.1
707 ascites, chylous 10.1
708 enterocolitis 10.1
709 galactorrhea 10.1
710 moyamoya disease 1 10.1
711 3-methylglutaconic aciduria, type iii 10.1
712 rheumatic fever-related antigen 10.1
713 hemophilia a 10.1
714 asthma 10.1
715 intraocular pressure quantitative trait locus 10.1
716 microvascular complications of diabetes 3 10.1
717 microvascular complications of diabetes 4 10.1
718 microvascular complications of diabetes 6 10.1
719 microvascular complications of diabetes 7 10.1
720 mannose-binding lectin deficiency 10.1
721 glucocorticoid resistance, generalized 10.1
722 autoimmune gastritis 10.1
723 livedoid vasculitis 10.1
724 metabolic acidosis 10.1
725 limb ischemia 10.1
726 sexual disorder 10.1
727 paroxysmal nocturnal hemoglobinuria 10.1
728 sialadenitis 10.1
729 lepromatous leprosy 10.1
730 intracranial aneurysm 10.1
731 chlamydia 10.1
732 pneumocystosis 10.1
733 portal vein thrombosis 10.1
734 gestational diabetes 10.1
735 iron deficiency anemia 10.1
736 coronary thrombosis 10.1
737 esophagitis 10.1
738 secondary hyperparathyroidism 10.1
739 acute leukemia 10.1
740 cardiovascular system disease 10.1
741 generalized anxiety disorder 10.1
742 normal pressure hydrocephalus 10.1
743 psychotic disorder 10.1
744 thymic carcinoma 10.1
745 coronary aneurysm 10.1
746 pleural empyema 10.1
747 mutism 10.1
748 eye disease 10.1
749 t-cell lymphoblastic leukemia/lymphoma 10.1
750 bacterial pneumonia 10.1
751 seborrheic dermatitis 10.1
752 cervix uteri carcinoma in situ 10.1
753 macroglobulinemia 10.1
754 orbital plasma cell granuloma 10.1
755 acquired angioedema 10.1
756 allergic encephalomyelitis 10.1
757 cervical intraepithelial neoplasia 10.1
758 coronary artery aneurysm 10.1
759 haemophilus influenzae 10.1
760 heparin-induced thrombocytopenia 10.1
761 leukemia, t-cell, chronic 10.1
762 microscopic polyangiitis 10.1
763 papular mucinosis 10.1
764 pemphigus foliaceus 10.1
765 spastic paraparesis 10.1
766 systemic onset juvenile idiopathic arthritis 10.1
767 dysautonomia 10.1
768 postherpetic neuralgia 10.1
769 syncope 10.1
770 angioedema, hereditary, type i 10.1
771 carpal tunnel syndrome 10.1
772 coronary artery dissection, spontaneous 10.1
773 prolidase deficiency 10.1
774 endocardial fibroelastosis 10.1
775 eosinophilic fasciitis 10.1
776 epidermodysplasia verruciformis 1 10.1
777 helicobacter pylori infection 10.1
778 pituitary adenoma, prolactin-secreting 10.1
779 gallbladder disease 1 10.1
780 branchiootic syndrome 1 10.1
781 anorexia nervosa 10.1
782 pulmonary disease, chronic obstructive 10.1
783 legionnaire disease 10.1
784 leukemia, acute lymphoblastic 10.1
785 tendinitis 10.1
786 cutaneous t cell lymphoma 10.1
787 atrial fibrillation 10.1
788 cardiac arrest 10.1
789 castleman disease 10.1
790 t cell deficiency 10.1
791 pyelonephritis 10.1
792 chagas disease 10.1
793 bronchopneumonia 10.1
794 nephrocalcinosis 10.1
795 tolosa-hunt syndrome 10.1
796 dementia 10.1
797 typhoid fever 10.1
798 hepatic infarction 10.1
799 sick sinus syndrome 10.1
800 autoimmune polyendocrine syndrome 10.1
801 frozen shoulder 10.1
802 communicating hydrocephalus 10.1
803 renovascular hypertension 10.1
804 heart septal defect 10.1
805 neovascular glaucoma 10.1
806 retinal vascular occlusion 10.1
807 melanoma 10.1
808 hyperinsulinism 10.1
809 drug-induced hepatitis 10.1
810 keratopathy 10.1
811 hemangioma 10.1
812 familial nephrotic syndrome 10.1
813 benign mesothelioma 10.1
814 euthyroid sick syndrome 10.1
815 bursitis 10.1
816 adenocarcinoma 10.1
817 churg-strauss syndrome 10.1
818 intracranial thrombosis 10.1
819 coronary stenosis 10.1
820 akinetic mutism 10.1
821 radiculopathy 10.1
822 tinea capitis 10.1
823 intracranial embolism 10.1
824 hypokalemia 10.1
825 brain edema 10.1
826 arteriosclerosis obliterans 10.1
827 inferior myocardial infarction 10.1
828 muscular atrophy 10.1
829 myeloid leukemia 10.1
830 vascular dementia 10.1
831 peliosis hepatis 10.1
832 acquired hemophilia a 10.1
833 acute graft versus host disease 10.1
834 autoimmune oophoritis 10.1
835 cold agglutinin disease 10.1
836 fasting hypoglycemia 10.1
837 malakoplakia 10.1
838 mycobacterium kansasii 10.1
839 foot drop 10.1
840 specific language disorder 10.1
841 familial chilblain lupus 10.1
842 acroosteolysis 10.0
843 burkitt lymphoma 10.0
844 fibromuscular dysplasia 10.0
845 renal cell carcinoma, nonpapillary 10.0
846 ige responsiveness, atopic 10.0
847 pityriasis rubra pilaris 10.0
848 lung cancer 10.0
849 aicardi-goutieres syndrome 1 10.0
850 hemolytic uremic syndrome, atypical 1 10.0
851 lymphoid interstitial pneumonia 10.0
852 pseudoxanthoma elasticum 10.0
853 macular degeneration, age-related, 1 10.0
854 meningioma, radiation-induced 10.0
855 meningioma, familial 10.0
856 resting heart rate, variation in 10.0
857 lung cancer susceptibility 3 10.0
858 gastric cancer 10.0
859 cyanosis, transient neonatal 10.0
860 peripartum cardiomyopathy 10.0
861 melanoma, cutaneous malignant 10 10.0
862 lambert-eaton myasthenic syndrome 10.0
863 vitamin b12 deficiency 10.0
864 marginal zone b-cell lymphoma 10.0
865 follicular lymphoma 10.0
866 autism spectrum disorder 10.0
867 collagenous colitis 10.0
868 ileitis 10.0
869 lung abscess 10.0
870 purpura fulminans 10.0
871 erythema elevatum diutinum 10.0
872 hyper ige syndrome 10.0
873 urolithiasis 10.0
874 dry eye syndrome 10.0
875 optic papillitis 10.0
876 cholelithiasis 10.0
877 chronic meningitis 10.0
878 glucose intolerance 10.0
879 placenta praevia 10.0
880 anogenital venereal wart 10.0
881 microcytic anemia 10.0
882 spinal meningioma 10.0
883 choroiditis 10.0
884 listeriosis 10.0
885 pulmonary alveolar proteinosis 10.0
886 pulmonary sarcoidosis 10.0
887 phaeohyphomycosis 10.0
888 bacteriuria 10.0
889 obstructive hydrocephalus 10.0
890 adult dermatomyositis 10.0
891 personality disorder 10.0
892 atrial heart septal defect 10.0
893 relapsing-remitting multiple sclerosis 10.0
894 basal cell carcinoma 10.0
895 proctitis 10.0
896 eosinophilic gastroenteritis 10.0
897 secondary syphilis 10.0
898 fibrous histiocytoma 10.0
899 secretory meningioma 10.0
900 lymphoplasmacyte-rich meningioma 10.0
901 intracranial hypotension 10.0
902 hypersplenism 10.0
903 acute disseminated encephalomyelitis 10.0
904 compartment syndrome 10.0
905 impetigo 10.0
906 erythema infectiosum 10.0
907 pyomyositis 10.0
908 chorioretinitis 10.0
909 atrophic gastritis 10.0
910 narcolepsy 10.0
911 viral infectious disease 10.0
912 epiglottitis 10.0
913 hypertensive encephalopathy 10.0
914 placental abruption 10.0
915 allergic angiitis 10.0
916 binswanger's disease 10.0
917 bowen's disease 10.0
918 chronic active epstein-barr virus infection 10.0
919 chronic thromboembolic pulmonary hypertension 10.0
920 homologous wasting disease 10.0
921 hypoaldosteronism 10.0
922 immunoglobulin g deficiency 10.0
923 lymphocytic hypophysitis 10.0
924 mycobacterium fortuitum 10.0
925 pure autonomic failure 10.0
926 pustular psoriasis 10.0
927 bunion 10.0
928 brain injury 10.0
929 acute adrenal insufficiency 10.0
930 refractory anemia 10.0
931 acute motor and sensory axonal neuropathy 10.0
932 polyendocrinopathy 10.0
933 hepatocellular carcinoma 9.9
934 cardiac conduction defect 9.9
935 chondrodysplasia punctata, tibia-metacarpal type 9.9
936 myelopathy, htlv-1-associated 9.9
937 neutrophil migration 9.9
938 obsessive-compulsive disorder 9.9
939 otitis media 9.9
940 ovarian cancer 9.9
941 pheochromocytoma 9.9
942 pneumothorax, primary spontaneous 9.9
943 prostate cancer 9.9
944 schizophrenia 9.9
945 thrombocytopenia 2 9.9
946 autism 9.9
947 complement component c1r/c1s deficiency 9.9
948 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.9
949 lysinuric protein intolerance 9.9
950 pancreatic cancer 9.9
951 periodontitis, chronic 9.9
952 thrombocytopenia 3 9.9
953 chondrodysplasia punctata 1, x-linked recessive 9.9
954 taqi polymorphism 9.9
955 thrombocytopenia 1 9.9
956 aging 9.9
957 cd4/cd8 t-cell ratio 9.9
958 leukemia, acute myeloid 9.9
959 reflex sympathetic dystrophy 9.9
960 huntington disease-like 3 9.9
961 huntington disease-like 2 9.9
962 aortic aneurysm, familial thoracic 1 9.9
963 endometrial cancer 9.9
964 avascular necrosis of femoral head, primary, 1 9.9
965 preterm premature rupture of the membranes 9.9
966 major affective disorder 8 9.9
967 major affective disorder 9 9.9
968 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.9
969 microcephaly, epilepsy, and diabetes syndrome 9.9
970 dengue virus 9.9
971 pregnancy loss, recurrent 1 9.9
972 leukemia, acute lymphoblastic 3 9.9
973 melioidosis 9.9
974 striatal degeneration, autosomal dominant 2 9.9
975 chlamydia pneumonia 9.9
976 bacterial sepsis 9.9
977 autoimmune glomerulonephritis 9.9
978 autoimmune vasculitis 9.9
979 extrapulmonary tuberculosis 9.9
980 autosomal recessive disease 9.9
981 adrenal gland pheochromocytoma 9.9
982 interleukin-7 receptor alpha deficiency 9.9
983 crest syndrome 9.9
984 nodal marginal zone lymphoma 9.9
985 non-alcoholic steatohepatitis 9.9
986 migraine with aura 9.9
987 venous insufficiency 9.9
988 thalassemia 9.9
989 tuberculoid leprosy 9.9
990 mumps 9.9
991 tonsillitis 9.9
992 pleural tuberculosis 9.9
993 gastric ulcer 9.9
994 lipoid nephrosis 9.9
995 ovarian disease 9.9
996 enophthalmos 9.9
997 erysipelas 9.9
998 lemierre's syndrome 9.9
999 cicatricial pemphigoid 9.9
1000 nephrosclerosis 9.9
1001 dysgammaglobulinemia 9.9
1002 tinea corporis 9.9
1003 miller fisher syndrome 9.9
1004 acute proliferative glomerulonephritis 9.9
1005 coccidioidomycosis 9.9
1006 tuberous sclerosis 9.9
1007 obstructive jaundice 9.9
1008 hypermobility syndrome 9.9
1009 splenic artery aneurysm 9.9
1010 algoneurodystrophy 9.9
1011 bipolar i disorder 9.9
1012 anus cancer 9.9
1013 selective igg deficiency disease 9.9
1014 azoospermia 9.9
1015 fungal infectious disease 9.9
1016 hemorrhagic disease 9.9
1017 granulomatous hepatitis 9.9
1018 hidradenitis suppurativa 9.9
1019 hidradenitis 9.9
1020 blepharoconjunctivitis 9.9
1021 nonspecific interstitial pneumonia 9.9
1022 hemoglobinopathy 9.9
1023 severe acute respiratory syndrome 9.9
1024 kidney cortex necrosis 9.9
1025 anuria 9.9
1026 allergic contact dermatitis 9.9
1027 acute porphyria 9.9
1028 mucinoses 9.9
1029 tropical spastic paraparesis 9.9
1030 neurodermatitis 9.9
1031 bipolar disorder 9.9
1032 sagittal sinus thrombosis 9.9
1033 bladder disease 9.9
1034 plexopathy 9.9
1035 plasmacytoma 9.9
1036 granuloma annulare 9.9
1037 insulinoma 9.9
1038 agnosia 9.9
1039 acneiform dermatitis 9.9
1040 cutaneous fibrous histiocytoma 9.9
1041 subacute bacterial endocarditis 9.9
1042 endophthalmitis 9.9
1043 arteriolosclerosis 9.9
1044 aortic disease 9.9
1045 dystonia 9.9
1046 retinal disease 9.9
1047 brown-sequard syndrome 9.9
1048 mitral valve disease 9.9
1049 anterior spinal artery syndrome 9.9
1050 diverticulitis 9.9
1051 active peptic ulcer disease 9.9
1052 gastrointestinal system disease 9.9
1053 chronic fatigue syndrome 9.9
1054 perinatal necrotizing enterocolitis 9.9
1055 in situ carcinoma 9.9
1056 parapsoriasis 9.9
1057 hypersensitivity vasculitis 9.9
1058 ankrd26-related thrombocytopenia 9.9
1059 autoimmune encephalitis 9.9
1060 autoimmune retinopathy 9.9
1061 dense deposit disease 9.9
1062 exfoliative dermatitis 9.9
1063 fibrillary glomerulonephritis 9.9
1064 htlv-1 associated myelopathy/tropical spastic paraparesis 9.9
1065 mycobacterium chelonae 9.9
1066 oral leukoplakia 9.9
1067 prurigo nodularis 9.9
1068 stenotrophomonas maltophilia infection 9.9
1069 paraneoplastic syndromes 9.9
1070 cerebrofacial arteriovenous metameric syndrome 9.9
1071 inflammatory myopathy with abundant macrophages 9.9
1072 periodic paralysis 9.9
1073 fixed drug eruption 9.9
1074 spontaneous intracranial hypotension 9.9
1075 pauci-immune glomerulonephritis 9.9
1076 premature aging 9.9
1077 rare tumor 9.9
1078 cytophagic histiocytic panniculitis 9.9
1079 alcohol dependence 9.9
1080 anal canal carcinoma 9.9
1081 gastroesophageal reflux 9.9
1082 aortic valve disease 1 9.9
1083 major affective disorder 1 9.9
1084 erythermalgia, primary 9.9
1085 exudative vitreoretinopathy 1 9.9
1086 immunoglobulin a deficiency 1 9.9
1087 attention deficit-hyperactivity disorder 9.9
1088 hypercalcemia, infantile, 1 9.9
1089 ichthyosis vulgaris 9.9
1090 kaposi sarcoma 9.9
1091 marfan syndrome 9.9
1092 melkersson-rosenthal syndrome 9.9
1093 mesothelioma, malignant 9.9
1094 neutrophilia, hereditary 9.9
1095 ocular cicatricial pemphigoid 9.9
1096 paroxysmal extreme pain disorder 9.9
1097 parkinson disease, late-onset 9.9
1098 protoporphyria, erythropoietic, 1 9.9
1099 pulmonary fibrosis, idiopathic 9.9
1100 retinoblastoma 9.9
1101 stiff-person syndrome 9.9
1102 trigeminal neuralgia 9.9
1103 tuberous sclerosis 1 9.9
1104 suppressor of tumorigenicity 3 9.9
1105 afibrinogenemia, congenital 9.9
1106 alopecia universalis congenita 9.9
1107 atrioventricular dissociation 9.9
1108 atrophoderma vermiculata 9.9
1109 australia antigen 9.9
1110 bloom syndrome 9.9
1111 cystic fibrosis 9.9
1112 hydrocephalus, congenital, 1 9.9
1113 dubin-johnson syndrome 9.9
1114 myxedema 9.9
1115 pituitary hormone deficiency, combined, 2 9.9
1116 pulmonic stenosis 9.9
1117 reticulum cell sarcoma 9.9
1118 retinitis pigmentosa 9.9
1119 xeroderma pigmentosum, variant type 9.9
1120 body mass index quantitative trait locus 11 9.9
1121 fragile x syndrome 9.9
1122 wiskott-aldrich syndrome 9.9
1123 fabry disease 9.9
1124 granulomatous disease, chronic, x-linked 9.9
1125 retinitis pigmentosa-deafness syndrome 9.9
1126 body mass index quantitative trait locus 9 9.9
1127 body mass index quantitative trait locus 8 9.9
1128 langerhans cell histiocytosis 9.9
1129 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.9
1130 nasopharyngeal carcinoma 9.9
1131 body mass index quantitative trait locus 4 9.9
1132 body mass index quantitative trait locus 10 9.9
1133 hypertensive nephropathy 9.9
1134 body mass index quantitative trait locus 7 9.9
1135 carotid intimal medial thickness 2 9.9
1136 celiac disease 3 9.9
1137 thrombocytopenia 4 9.9
1138 diabetes mellitus, ketosis-prone 9.9
1139 body mass index quantitative trait locus 12 9.9
1140 factor xi deficiency 9.9
1141 body mass index quantitative trait locus 14 9.9
1142 microvascular complications of diabetes 5 9.9
1143 antithrombin iii deficiency 9.9
1144 alpha-1-antitrypsin deficiency 9.9
1145 complement component 8 deficiency, type i 9.9
1146 complement component 9 deficiency 9.9
1147 complement component 4b deficiency 9.9
1148 aortic valve disease 2 9.9
1149 human herpesvirus 8 9.9
1150 body mass index quantitative trait locus 18 9.9
1151 autoimmune lymphoproliferative syndrome, type iii 9.9
1152 thrombocytopenia 5 9.9
1153 thrombocytopenia 6 9.9
1154 helix syndrome 9.9
1155 body mass index quantitative trait locus 19 9.9
1156 body mass index quantitative trait locus 20 9.9
1157 tendinopathy 9.9
1158 adrenal cortical carcinoma 9.9
1159 autoimmune peripheral neuropathy 9.9
1160 autoimmune pancreatitis 9.9
1161 chikungunya 9.9
1162 autoimmune polyendocrine syndrome type 1 9.9
1163 granulomatous amebic encephalitis 9.9
1164 hypophosphatemia 9.9
1165 restless legs syndrome 9.9
1166 usher syndrome 9.9
1167 variola major 9.9
1168 adult t-cell leukemia 9.9
1169 chorioamnionitis 9.9
1170 first-degree atrioventricular block 9.9
1171 sinoatrial node disease 9.9
1172 sleep apnea 9.9
1173 renal fibrosis 9.9
1174 inflammatory myofibroblastic tumor 9.9
1175 apraxia 9.9
1176 cogan syndrome 9.9
1177 agraphia 9.9
1178 basal ganglia calcification 9.9
1179 gallbladder disease 9.9
1180 x-linked chondrodysplasia punctata 1 9.9
1181 ectopic pregnancy 9.9
1182 left ventricular noncompaction 9.9
1183 myoglobinuria 9.9
1184 meningococcal meningitis 9.9
1185 chronic myelomonocytic leukemia 9.9
1186 non-alcoholic fatty liver disease 9.9
1187 polycystic kidney disease 9.9
1188 rasopathy 9.9
1189 pelvic inflammatory disease 9.9
1190 cysticercosis 9.9
1191 trypanosomiasis 9.9
1192 aortic atherosclerosis 9.9
1193 left bundle branch hemiblock 9.9
1194 asbestosis 9.9
1195 common cold 9.9
1196 diaphragm disease 9.9
1197 methemoglobinemia 9.9
1198 microcephaly 9.9
1199 dissociative disorder 9.9
1200 spastic diplegia 9.9
1201 corneal edema 9.9
1202 q fever 9.9
1203 pertussis 9.9
1204 allergic conjunctivitis 9.9
1205 social phobia 9.9
1206 cat-scratch disease 9.9
1207 retinal microaneurysm 9.9
1208 horner's syndrome 9.9
1209 chondrocalcinosis 9.9
1210 hypertensive retinopathy 9.9
1211 listeria meningitis 9.9
1212 cauda equina syndrome 9.9
1213 palindromic rheumatism 9.9
1214 ischemic neuropathy 9.9
1215 conn's syndrome 9.9
1216 superficial keratitis 9.9
1217 dengue disease 9.9
1218 marasmus 9.9
1219 vulva cancer 9.9
1220 hepatic coma 9.9
1221 acute kidney tubular necrosis 9.9
1222 paracoccidioidomycosis 9.9
1223 migraine without aura 9.9
1224 hypochondriasis 9.9
1225 endomyocardial fibrosis 9.9
1226 ehlers-danlos syndrome 9.9
1227 skin sarcoidosis 9.9
1228 hepatic encephalopathy 9.9
1229 posterior scleritis 9.9
1230 panophthalmitis 9.9
1231 iritis 9.9
1232 acute retrobulbar neuritis 9.9
1233 suppurative thyroiditis 9.9
1234 acute thyroiditis 9.9
1235 gonadal dysgenesis 9.9
1236 neuroleptic malignant syndrome 9.9
1237 chorea gravidarum 9.9
1238 avoidant personality disorder 9.9
1239 nodular nonsuppurative panniculitis 9.9
1240 chromoblastomycosis 9.9
1241 dermatomycosis 9.9
1242 ectropion 9.9
1243 ventricular septal defect 9.9
1244 conversion disorder 9.9
1245 malignant fibrous histiocytoma 9.9
1246 telogen effluvium 9.9
1247 leiomyosarcoma 9.9
1248 chronic mucocutaneous candidiasis 9.9
1249 vulva squamous cell carcinoma 9.9
1250 dental caries 9.9
1251 vaginitis 9.9
1252 myeloproliferative neoplasm 9.9
1253 focal epilepsy 9.9
1254 prothrombin deficiency 9.9
1255 motor neuron disease 9.9
1256 neonatal jaundice 9.9
1257 wernicke encephalopathy 9.9
1258 gastric antral vascular ectasia 9.9
1259 kluver-bucy syndrome 9.9
1260 splenic abscess 9.9
1261 cervicitis 9.9
1262 kidney cancer 9.9
1263 irritant dermatitis 9.9
1264 parasitic protozoa infectious disease 9.9
1265 idiopathic interstitial pneumonia 9.9
1266 bruxism 9.9
1267 newcastle disease 9.9
1268 periarthritis 9.9
1269 substance abuse 9.9
1270 food allergy 9.9
1271 glioblastoma multiforme 9.9
1272 papillary carcinoma 9.9
1273 cutis laxa 9.9
1274 lipomatosis 9.9
1275 nemaline myopathy 9.9
1276 tracheal stenosis 9.9
1277 vaccinia 9.9
1278 teratoma 9.9
1279 hyperglobulinemic purpura 9.9
1280 temporal lobe epilepsy 9.9
1281 fibrosarcoma of bone 9.9
1282 palmoplantar keratosis 9.9
1283 laryngitis 9.9
1284 mammary paget's disease 9.9
1285 necrobiosis lipoidica 9.9
1286 turner syndrome 9.9
1287 lateral medullary syndrome 9.9
1288 gastric adenocarcinoma 9.9
1289 protein c deficiency 9.9
1290 anovulation 9.9
1291 porokeratosis 9.9
1292 shwartzman phenomenon 9.9
1293 pituitary adenoma 9.9
1294 merkel cell carcinoma 9.9
1295 restrictive cardiomyopathy 9.9
1296 pseudohypoparathyroidism 9.9
1297 polyradiculopathy 9.9
1298 neuromuscular disease 9.9
1299 dyslexia 9.9
1300 dysgerminoma 9.9
1301 dysgraphia 9.9
1302 large cell carcinoma 9.9
1303 familial retinoblastoma 9.9
1304 placenta accreta 9.9
1305 subacute glomerulonephritis 9.9
1306 poliomyelitis 9.9
1307 neurotic disorder 9.9
1308 prosopagnosia 9.9
1309 adjustment disorder 9.9
1310 ovarian cyst 9.9
1311 human immunodeficiency virus infectious disease 9.9
1312 pulmonary venoocclusive disease 9.9
1313 dysgerminoma of ovary 9.9
1314 verruciform xanthoma of skin 9.9
1315 cerebral lymphoma 9.9
1316 anterolateral myocardial infarction 9.9
1317 nephrolithiasis 9.9
1318 silent myocardial infarction 9.9
1319 pericardial mesothelioma 9.9
1320 central pontine myelinolysis 9.9
1321 anthrax disease 9.9
1322 delusional disorder 9.9
1323 mite infestation 9.9
1324 interstitial myocarditis 9.9
1325 actinomycosis 9.9
1326 bullous skin disease 9.9
1327 subcorneal pustular dermatosis 9.9
1328 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.9
1329 smallpox 9.9
1330 molluscum contagiosum 9.9
1331 cutaneous leishmaniasis 9.9
1332 homocystinuria 9.9
1333 priapism 9.9
1334 carotid artery dissection 9.9
1335 vitreous detachment 9.9
1336 deep keratitis 9.9
1337 follicular mucinosis 9.9
1338 steroid-induced glaucoma 9.9
1339 periostitis 9.9
1340 48, xxxx 9.9
1341 hereditary distal renal tubular acidosis 9.9
1342 hypermobile ehlers-danlos syndrome 9.9
1343 antisynthetase syndrome 9.9
1344 autoimmune myocarditis 9.9
1345 bronchopulmonary dysplasia 9.9
1346 central congenital hypothyroidism 9.9
1347 central serous chorioretinopathy 9.9
1348 complement component deficiency 9.9
1349 cutaneous sclerosis 9.9
1350 fibrosing mediastinitis 9.9
1351 germ cells tumors 9.9
1352 gigantism 9.9
1353 gigantomastia 9.9
1354 glioma 9.9
1355 human t-cell leukemia virus type 1 9.9
1356 lichen planus pemphigoides 9.9
1357 meningococcal infection 9.9
1358 muscular dystrophy white matter spongiosis 9.9
1359 mycobacterium abscessus 9.9
1360 neisseria meningitidis infection 9.9
1361 nephrogenic systemic fibrosis 9.9
1362 oral cancer 9.9
1363 primary agammaglobulinemia 9.9
1364 pseudobulbar affect 9.9
1365 rosai-dorfman disease 9.9
1366 soft tissue sarcoma 9.9
1367 spondylarthropathy 9.9
1368 sutton disease 2 9.9
1369 synovial chondromatosis 9.9
1370 thrombasthenia 9.9
1371 thunderclap headache 9.9
1372 complement component 8 deficiency 9.9
1373 cryptogenic cirrhosis 9.9
1374 pituitary tumors 9.9
1375 spinal cord injury 9.9
1376 paraneoplastic limbic encephalitis 9.9
1377 asbestos intoxication 9.9
1378 glial tumor 9.9
1379 adrenogenital syndrome 9.9
1380 vulvar intraepithelial neoplasia 9.9
1381 immune complex mediated vasculitis 9.9
1382 rare hereditary hemochromatosis 9.9
1383 idiopathic nephrotic syndrome 9.9
1384 pre-descemet corneal dystrophy 9.9
1385 tafro syndrome 9.9
1386 systemic polyarteritis nodosa 9.9
1387 postpartum psychosis 9.9
1388 secondary vasculitis 9.9
1389 acquired prothrombin deficiency 9.9
1390 non-inflammatory vasculopathy 9.9
1391 paraneoplastic pemphigus 9.9
1392 argyria 9.9
1393 secondary erythromelalgia 9.9
1394 solar urticaria 9.9
1395 overgrowth syndrome 9.9
1396 acute motor axonal neuropathy 9.9
1397 penicilliosis 9.8
1398 borderline personality disorder 9.8
1399 huntington disease 9.7
1400 st. louis encephalitis 9.7
1401 rabies 9.7
1402 abducens palsy 9.7
1403 ainhum 9.7
1404 diamond-blackfan anemia 1 9.7
1405 antiphospholipid syndrome, familial 9.7
1406 aplasia cutis congenita, nonsyndromic 9.7
1407 alopecia, androgenetic, 1 9.7
1408 leukemia, chronic lymphocytic 2 9.7
1409 cardiac arrhythmia 9.7
1410 hypercarotenemia and vitamin a deficiency, autosomal dominant 9.7
1411 centralopathic epilepsy 9.7
1412 clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly 9.7
1413 seizures, benign familial neonatal, 1 9.7
1414 coproporphyria, hereditary 9.7
1415 creutzfeldt-jakob disease 9.7
1416 diabetes insipidus, nephrogenic, autosomal 9.7
1417 dyschromatosis symmetrica hereditaria 9.7
1418 dementia, lewy body 9.7
1419 eosinophilopenia 9.7
1420 facial hypertrichosis 9.7
1421 hemifacial atrophy, progressive 9.7
1422 periodic fever, familial, autosomal dominant 9.7
1423 developmental dysplasia of the hip 1 9.7
1424 gilbert syndrome 9.7
1425 endosteal hyperostosis, autosomal dominant 9.7
1426 chromosome 18p deletion syndrome 9.7
1427 multiple system atrophy 1 9.7
1428 kabuki syndrome 1 9.7
1429 leiomyoma, uterine 9.7
1430 lentigines 9.7
1431 treacher collins syndrome 1 9.7
1432 meniere disease 9.7
1433 moebius syndrome 9.7
1434 renal failure, progressive, with hypertension 9.7
1435 cyclic neutropenia 9.7
1436 hypokalemic periodic paralysis, type 1 9.7
1437 platelet aggregation, spontaneous 9.7
1438 platelet groups--ko system 9.7
1439 polydactyly, preaxial i 9.7
1440 polydactyly, preaxial iii 9.7
1441 polydactyly, preaxial iv 9.7
1442 actinic prurigo 9.7
1443 prader-willi syndrome 9.7
1444 pelvic organ prolapse 9.7
1445 schistosoma mansoni infection, susceptibility/ 9.7
1446 keratosis, seborrheic 9.7
1447 neural tube defects 9.7
1448 spinocerebellar ataxia 6 9.7
1449 strabismus 9.7
1450 tetralogy of fallot 9.7
1451 thyroid cancer, nonmedullary, 1 9.7
1452 torticollis 9.7
1453 trichomegaly 9.7
1454 trichorhinophalangeal syndrome, type i 9.7
1455 vasculopathy, retinal, with cerebral leukodystrophy 9.7
1456 vesicoureteral reflux 1 9.7
1457 volvulus of midgut 9.7
1458 von willebrand disease, type 1 9.7
1459 white sponge nevus 1 9.7
1460 wolff-parkinson-white syndrome 9.7
1461 acid phosphatase deficiency 9.7
1462 adrenocortical carcinoma, hereditary 9.7
1463 hermansky-pudlak syndrome 1 9.7
1464 alstrom syndrome 9.7
1465 anemia, hypochromic microcytic, with iron overload 1 9.7
1466 chediak-higashi syndrome 9.7
1467 citrullinemia, classic 9.7
1468 cryptorchidism, unilateral or bilateral 9.7
1469 cutis marmorata telangiectatica congenita 9.7
1470 duodenal atresia 9.7
1471 fibrosclerosis, multifocal 9.7
1472 goodpasture syndrome 9.7
1473 factor xii deficiency 9.7
1474 pulmonary venoocclusive disease 2, autosomal recessive 9.7
1475 hyperlipoproteinemia, type i 9.7
1476 hypoadrenocorticism, familial 9.7
1477 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 9.7
1478 papillon-lefevre syndrome 9.7
1479 mannosidosis, alpha b, lysosomal 9.7
1480 spondylometaphyseal dysplasia, sedaghatian type 9.7
1481 oculocerebral syndrome with hypopigmentation 9.7
1482 nonarteritic anterior ischemic optic neuropathy 9.7
1483 osteogenic sarcoma 9.7
1484 pancreatic agenesis 1 9.7
1485 interstitial pneumonitis, desquamative, familial 9.7
1486 polycythemia vera 9.7
1487 gitelman syndrome 9.7
1488 pulmonary venoocclusive disease 1, autosomal dominant 9.7
1489 respiratory distress syndrome in premature infants 9.7
1490 insulin-like growth factor i 9.7
1491 oliver-mcfarlane syndrome 9.7
1492 vascular hyalinosis 9.7
1493 werner syndrome 9.7
1494 xeroderma pigmentosum, complementation group c 9.7
1495 adrenoleukodystrophy 9.7
1496 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 9.7
1497 incontinentia pigmenti 9.7
1498 mental retardation with optic atrophy, deafness, and seizures 9.7
1499 mucopolysaccharidosis, type ii 9.7
1500 premature ovarian failure 1 9.7
1501 paine syndrome 9.7
1502 androgen insensitivity, partial 9.7
1503 retinitis pigmentosa 11 9.7
1504 short tarsus with absence of lower eyelashes 9.7
1505 frontotemporal dementia 9.7
1506 agammaglobulinemia 1, autosomal recessive 9.7
1507 wilms tumor 5 9.7
1508 bile duct cysts 9.7
1509 graves disease 2 9.7
1510 light fixation seizure syndrome 9.7
1511 brittle bone disorder 9.7
1512 ventricular fibrillation, paroxysmal familial, 1 9.7
1513 panbronchiolitis, diffuse 9.7
1514 abdominal obesity-metabolic syndrome 1 9.7
1515 transaldolase deficiency 9.7
1516 diamond-blackfan anemia 2 9.7
1517 pars planitis 9.7
1518 inflammatory bowel disease 5 9.7
1519 lymphangioleiomyomatosis 9.7
1520 spermatogenic failure 3 9.7
1521 creatinine clearance quantitative trait locus 9.7
1522 patent ductus arteriosus 1 9.7
1523 hypereosinophilic syndrome, idiopathic 9.7
1524 noonan syndrome-like disorder with loose anagen hair 1 9.7
1525 juvenile myelomonocytic leukemia 9.7
1526 autoimmune disease 1 9.7
1527 psoriasis 9 9.7
1528 aspirin resistance 9.7
1529 leukemia, chronic myeloid 9.7
1530 phobia, specific 9.7
1531 autoimmune disease 2 9.7
1532 autoimmune disease 3 9.7
1533 lipodystrophy, partial, acquired 9.7
1534 syndactyly, mesoaxial synostotic, with phalangeal reduction 9.7
1535 migraine with or without aura 8 9.7
1536 complement component 7 deficiency 9.7
1537 pulmonary alveolar proteinosis, acquired 9.7
1538 colorectal cancer 2 9.7
1539 inflammatory bowel disease 14 9.7
1540 hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy 9.7
1541 acute promyelocytic leukemia 9.7
1542 psoriasis 10 9.7
1543 complement component 6 deficiency 9.7
1544 premature ovarian failure 7 9.7
1545 schizophrenia 13 9.7
1546 purine nucleoside phosphorylase deficiency 9.7
1547 trichotillomania 9.7
1548 fatty liver disease, nonalcoholic 1 9.7
1549 reynolds syndrome 9.7
1550 myxoid liposarcoma 9.7
1551 prothrombin deficiency, congenital 9.7
1552 ficolin 3 deficiency 9.7
1553 okt4 epitope deficiency 9.7
1554 beta-thalassemia 9.7
1555 muscle hypertrophy 9.7
1556 psoriasis 14, pustular 9.7
1557 ras-associated autoimmune leukoproliferative disorder 9.7
1558 leptin deficiency or dysfunction 9.7
1559 alacrima, achalasia, and mental retardation syndrome 9.7
1560 cholangiocarcinoma 9.7
1561 pachyonychia congenita 3 9.7
1562 carbonic anhydrase va deficiency, hyperammonemia due to 9.7
1563 nephrotic syndrome, type 10 9.7
1564 analbuminemia 9.7
1565 hydrops, lactic acidosis, and sideroblastic anemia 9.7
1566 portal hypertension, noncirrhotic 9.7
1567 mucopolysaccharidosis-plus syndrome 9.7
1568 nephrotic syndrome, type 17 9.7
1569 nephrotic syndrome, type 19 9.7
1570 mucocutaneous ulceration, chronic 9.7
1571 peyronie's disease 9.7
1572 sydenham chorea 9.7
1573 corticosteroid allergy 9.7
1574 sulfonamide allergy 9.7
1575 streptococcus pneumonia 9.7
1576 autoimmune optic neuritis 9.7
1577 hirata disease 9.7
1578 aspiration pneumonia 9.7
1579 nipah virus encephalitis 9.7
1580 swine influenza 9.7
1581 primary amebic meningoencephalitis 9.7
1582 trichosporonosis 9.7
1583 brachydactyly 9.7
1584 tooth agenesis 9.7
1585 abdominal tuberculosis 9.7
1586 oculocutaneous albinism 9.7
1587 hypochromic microcytic anemia 9.7
1588 small cell carcinoma 9.7
1589 anaplastic large cell lymphoma 9.7
1590 peripheral t-cell lymphoma 9.7
1591 t-cell large granular lymphocyte leukemia 9.7
1592 androgenic alopecia 9.7
1593 hepatocellular adenoma 9.7
1594 villous adenoma 9.7
1595 fibroma 9.7
1596 withdrawal disorder 9.7
1597 cd40 ligand deficiency 9.7
1598 munchausen by proxy 9.7
1599 marantic endocarditis 9.7
1600 brain glioma 9.7
1601 heavy chain disease 9.7
1602 anosognosia 9.7
1603 autotopagnosia 9.7
1604 finger agnosia 9.7
1605 visual agnosia 9.7
1606 microscopic colitis 9.7
1607 stuttering 9.7
1608 scoliosis 9.7
1609 sclerosteosis 9.7
1610 angular cheilitis 9.7
1611 oral hairy leukoplakia 9.7
1612 mastoiditis 9.7
1613 respiratory allergy 9.7
1614 pollen allergy 9.7
1615 metal allergy 9.7
1616 penicillin allergy 9.7
1617 dextro-looped transposition of the great arteries 9.7
1618 hereditary lymphedema i 9.7
1619 ocular tuberculosis 9.7
1620 bone disease 9.7
1621 physical disorder 9.7
1622 acquired generalized lipodystrophy 9.7
1623 igg4-related disease 9.7
1624 bone sarcoma 9.7
1625 middle east respiratory syndrome 9.7
1626 multicentric castleman disease 9.7
1627 postural orthostatic tachycardia syndrome 9.7
1628 asymptomatic neurosyphilis 9.7
1629 syphilitic meningitis 9.7
1630 sleeping sickness 9.7
1631 viral meningitis 9.7
1632 hypopyon 9.7
1633 microphthalmia 9.7
1634 cystinosis 9.7
1635 open-angle glaucoma 9.7
1636 hypertrophy of breast 9.7
1637 paragonimiasis 9.7
1638 cerebral lipidosis 9.7
1639 fiedler's myocarditis 9.7
1640 mesenteric lymphadenitis 9.7
1641 filariasis 9.7
1642 salivary gland disease 9.7
1643 abducens nerve disease 9.7
1644 hypospadias 9.7
1645 amnestic disorder 9.7
1646 obsessive-compulsive personality disorder 9.7
1647 alport syndrome 9.7
1648 discitis 9.7
1649 leech infestation 9.7
1650 pulpitis 9.7
1651 anhidrosis 9.7
1652 common wart 9.7
1653 acute orbital inflammation 9.7
1654 orbital cellulitis 9.7
1655 vitamin k deficiency bleeding 9.7
1656 keratomalacia 9.7
1657 arteriovenous malformation 9.7
1658 gingival recession 9.7
1659 epidural abscess 9.7
1660 subdural empyema 9.7
1661 xanthogranulomatous pyelonephritis 9.7
1662 fissured tongue 9.7
1663 oculomotor nerve paralysis 9.7
1664 infant gynecomastia 9.7
1665 polycystic ovary syndrome 9.7
1666 hyperandrogenism 9.7
1667 patau syndrome 9.7
1668 familial hyperlipidemia 9.7
1669 choledocholithiasis 9.7
1670 blind hypotensive eye 9.7
1671 multicentric reticulohistiocytosis 9.7
1672 clubfoot 9.7
1673 coronary artery vasospasm 9.7
1674 ecthyma 9.7
1675 osteopoikilosis 9.7
1676 panuveitis 9.7
1677 low compliance bladder 9.7
1678 pseudoretinitis pigmentosa 9.7
1679 descending colon cancer 9.7
1680 dengue hemorrhagic fever 9.7
1681 male infertility 9.7
1682 varicocele 9.7
1683 balantidiasis 9.7
1684 kleptomania 9.7
1685 secondary hyperparathyroidism of renal origin 9.7
1686 blood coagulation disease 9.7
1687 bell's palsy 9.7
1688 retinal ischemia 9.7
1689 olecranon bursitis 9.7
1690 pyloric stenosis 9.7
1691 blastomycosis 9.7
1692 pseudobulbar palsy 9.7
1693 gynecomastia 9.7
1694 leiomyoma 9.7
1695 nephronophthisis 9.7
1696 newborn respiratory distress syndrome 9.7
1697 cerebral atherosclerosis 9.7
1698 hypercementosis 9.7
1699 cicatricial ectropion 9.7
1700 thyroid crisis 9.7
1701 mikulicz disease 9.7
1702 carotid stenosis 9.7
1703 vertebrobasilar insufficiency 9.7
1704 lobomycosis 9.7
1705 relapsing fever 9.7
1706 renal osteodystrophy 9.7
1707 eumycotic mycetoma 9.7
1708 periventricular leukomalacia 9.7
1709 paronychia 9.7
1710 esophageal candidiasis 9.7
1711 dissociated nystagmus 9.7
1712 megaesophagus 9.7
1713 brain cancer 9.7
1714 cutaneous porphyria 9.7
1715 klebsiella pneumonia 9.7
1716 intestinal tuberculosis 9.7
1717 congenital toxoplasmosis 9.7
1718 urethritis 9.7
1719 osteopetrosis 9.7
1720 patent foramen ovale 9.7
1721 sapho syndrome 9.7
1722 beriberi 9.7
1723 familial hypercholesterolemia 9.7
1724 acute closed-angle glaucoma 9.7
1725 necrotizing ulcerative gingivitis 9.7
1726 schistosomiasis 9.7
1727 peptic esophagitis 9.7
1728 rubeosis iridis 9.7
1729 alcoholic liver cirrhosis 9.7
1730 poems syndrome 9.7
1731 neonatal myasthenia gravis 9.7
1732 blue toe syndrome 9.7
1733 oral candidiasis 9.7
1734 pulmonary valve insufficiency 9.7
1735 suppurative cholangitis 9.7
1736 capillary leak syndrome 9.7
1737 autosomal dominant cerebellar ataxia 9.7
1738 sclerosing keratitis 9.7
1739 pemphigoid gestationis 9.7
1740 sporotrichosis 9.7
1741 niemann-pick disease 9.7
1742 reye syndrome 9.7
1743 geographic tongue 9.7
1744 glossitis 9.7
1745 aggressive periodontitis 9.7
1746 lymphangioma 9.7
1747 disease of mental health 9.7
1748 chronic cervicitis 9.7
1749 arthus reaction 9.7
1750 respiratory system disease 9.7
1751 acute chest syndrome 9.7
1752 endogenous depression 9.7
1753 central nervous system tuberculosis 9.7
1754 duodenal ulcer 9.7
1755 facial hemiatrophy 9.7
1756 neuroendocrine carcinoma 9.7
1757 cerebral palsy 9.7
1758 encephalomalacia 9.7
1759 hyperostosis 9.7
1760 acute maxillary sinusitis 9.7
1761 maxillary sinusitis 9.7
1762 transient arthritis 9.7
1763 blood platelet disease 9.7
1764 ankylosis 9.7
1765 monoclonal paraproteinemia 9.7
1766 generalized atherosclerosis 9.7
1767 west nile encephalitis 9.7
1768 acromegaly 9.7
1769 opportunistic mycosis 9.7
1770 chronic conjunctivitis 9.7
1771 motor peripheral neuropathy 9.7
1772 hematologic cancer 9.7
1773 pancreas disease 9.7
1774 cystadenoma 9.7
1775 ovarian brenner tumor 9.7
1776 perivascular epithelioid cell tumor 9.7
1777 transitional cell carcinoma 9.7
1778 pigmented villonodular synovitis 9.7
1779 hemangioma of liver 9.7
1780 hemopneumothorax 9.7
1781 cerebellar disease 9.7
1782 acute interstitial pneumonia 9.7
1783 long qt syndrome 9.7
1784 endometrial adenocarcinoma 9.7
1785 aleutian mink disease 9.7
1786 cockayne syndrome 9.7
1787 acinar cell carcinoma 9.7
1788 cystadenocarcinoma 9.7
1789 papillary adenocarcinoma 9.7
1790 scleredema adultorum 9.7
1791 spinal cord disease 9.7
1792 neurilemmoma 9.7
1793 aspiration pneumonitis 9.7
1794 encapsulated thymoma 9.7
1795 teratocarcinoma 9.7
1796 benign epilepsy with centrotemporal spikes 9.7
1797 liposarcoma 9.7
1798 carotid artery disease 9.7
1799 breast adenocarcinoma 9.7
1800 breast disease 9.7
1801 signet ring cell adenocarcinoma 9.7
1802 pancreatic ductal adenocarcinoma 9.7
1803 mastocytosis 9.7
1804 brain stem infarction 9.7
1805 superior mesenteric artery syndrome 9.7
1806 cavernous sinus thrombosis 9.7
1807 choriocarcinoma 9.7
1808 mast cell neoplasm 9.7
1809 brachial plexus neuropathy 9.7
1810 extramedullary plasmacytoma 9.7
1811 hermansky-pudlak syndrome 9.7
1812 lynch syndrome 9.7
1813 lung squamous cell carcinoma 9.7
1814 adrenal cortical adenocarcinoma 9.7
1815 loeffler endocarditis 9.7
1816 bladder urothelial carcinoma 9.7
1817 lymphocytic gastritis 9.7
1818 gastrointestinal tuberculosis 9.7
1819 tricuspid valve stenosis 9.7
1820 echolalia 9.7
1821 glucose metabolism disease 9.7
1822 burning mouth syndrome 9.7
1823 tinea favosa 9.7
1824 schnitzler syndrome 9.7
1825 neuromuscular junction disease 9.7
1826 seminoma 9.7
1827 clear cell renal cell carcinoma 9.7
1828 hypotrichosis 9.7
1829 nominal aphasia 9.7
1830 ludwig's angina 9.7
1831 hydranencephaly 9.7
1832 ideomotor apraxia 9.7
1833 cervical adenitis 9.7
1834 extracutaneous mastocytoma 9.7
1835 extragonadal germ cell cancer 9.7
1836 somatoform disorder 9.7
1837 anti-basement membrane glomerulonephritis 9.7
1838 cavernous hemangioma 9.7
1839 intrahepatic cholangiocarcinoma 9.7
1840 adenocarcinoma in situ 9.7
1841 gerstmann syndrome 9.7
1842 ureteral obstruction 9.7
1843 heart sarcoma 9.7
1844 blepharospasm 9.7
1845 intestinal disease 9.7
1846 pituitary gland disease 9.7
1847 gingival hypertrophy 9.7
1848 pulmonary coin lesion 9.7
1849 keratinizing squamous cell carcinoma 9.7
1850 anal squamous cell carcinoma 9.7
1851 acute pyelonephritis 9.7
1852 third cranial nerve disease 9.7
1853 diffuse pulmonary fibrosis 9.7
1854 agoraphobia 9.7
1855 panic disorder 9.7
1856 inflammatory breast carcinoma 9.7
1857 acral lentiginous melanoma 9.7
1858 viral encephalitis 9.7
1859 plasma cell neoplasm 9.7
1860 adrenal adenoma 9.7
1861 diffuse idiopathic skeletal hyperostosis 9.7
1862 spinal stenosis 9.7
1863 bilateral breast cancer 9.7
1864 mediastinal malignant lymphoma 9.7
1865 inverted follicular keratosis 9.7
1866 mitochondrial myopathy 9.7
1867 subacute thyroiditis 9.7
1868 nodular episcleritis 9.7
1869 peptic ulcer perforation 9.7
1870 bladder tuberculosis 9.7
1871 stomach disease 9.7
1872 parathyroid adenoma 9.7
1873 intraocular lymphoma 9.7
1874 hemarthrosis 9.7
1875 carotid artery occlusion 9.7
1876 extrinsic allergic alveolitis 9.7
1877 polycythemia 9.7
1878 retinal degeneration 9.7
1879 polyhydramnios 9.7
1880 impetigo herpetiformis 9.7
1881 acute cor pulmonale 9.7
1882 lip cancer 9.7
1883 gastroduodenitis 9.7
1884 hodgkin's lymphoma, mixed cellularity 9.7
1885 eating disorder 9.7
1886 fasciolopsiasis 9.7
1887 lower lip cancer 9.7
1888 skin melanoma 9.7
1889 sideroblastic anemia 9.7
1890 autosomal dominant polycystic kidney disease 9.7
1891 liver lymphoma 9.7
1892 gastrointestinal lymphoma 9.7
1893 eczema herpeticum 9.7
1894 achalasia 9.7
1895 speech disorder 9.7
1896 ocular hypertension 9.7
1897 mechanical strabismus 9.7
1898 hypopituitarism 9.7
1899 exposure keratitis 9.7
1900 dacryoadenitis 9.7
1901 dextrocardia 9.7
1902 episodic ataxia 9.7
1903 babesiosis 9.7
1904 purulent endophthalmitis 9.7
1905 renal tuberculosis 9.7
1906 diabetic neuropathy 9.7
1907 diastolic heart failure 9.7
1908 irritable bowel syndrome 9.7
1909 myositis fibrosa 9.7
1910 toxocariasis 9.7
1911 tuberculous peritonitis 9.7
1912 refractive error 9.7
1913 lingual-facial-buccal dyskinesia 9.7
1914 interstitial keratitis 9.7
1915 toxic maculopathy 9.7
1916 cardiovascular syphilis 9.7
1917 median arcuate ligament syndrome 9.7
1918 villonodular synovitis 9.7
1919 waterhouse-friderichsen syndrome 9.7
1920 hypervitaminosis d 9.7
1921 albinism 9.7
1922 keloid disorder 9.7
1923 triple x syndrome 9.7
1924 15q duplication syndrome and related disorders 9.7
1925 cytochrome p450 oxidoreductase deficiency 9.7
1926 genetic atypical hemolytic-uremic syndrome 9.7
1927 mitochondrial disorders 9.7
1928 trichorhinophalangeal syndrome 9.7
1929 aberrant subclavian artery 9.7
1930 acquired amegakaryocytic thrombocytopenia 9.7
1931 actinic cheilitis 9.7
1932 acute monoblastic leukemia 9.7
1933 acute mountain sickness 9.7
1934 adrenomyeloneuropathy 9.7
1935 angioimmunoblastic lymphadenopathy with dysproteinemia 9.7
1936 anton's syndrome 9.7
1937 aquagenic pruritus 9.7
1938 athetosis 9.7
1939 bk-virus nephropathy 9.7
1940 blastic plasmacytoid dendritic cell 9.7
1941 bone marrow necrosis 9.7
1942 bowenoid papulosis 9.7
1943 broken heart syndrome 9.7
1944 carcinoma showing thymus-like differentiation 9.7
1945 cardiac rupture 9.7
1946 cataract-glaucoma 9.7
1947 cavernous lymphangioma 9.7
1948 cerebellar degeneration 9.7
1949 cerebrospinal fluid leak 9.7
1950 cluster headache 9.7
1951 cold urticaria 9.7
1952 congenital cytomegalovirus 9.7
1953 congenital human immunodeficiency virus 9.7
1954 corticobasal degeneration 9.7
1955 cryofibrinogenemia 9.7
1956 cutaneous larva migrans 9.7
1957 dendritic cell tumor 9.7
1958 dentinogenesis imperfecta type 2 9.7
1959 double discordia 9.7
1960 drug reaction with eosinophilia and systemic symptoms 9.7
1961 dwarfism 9.7
1962 embryonal sarcoma 9.7
1963 giant cell myocarditis 9.7
1964 granulomatous lobular mastitis 9.7
1965 guttate psoriasis 9.7
1966 hashimoto encephalopathy 9.7
1967 hemangioendothelioma 9.7
1968 hemorrhagic proctocolitis 9.7
1969 herpes simplex encephalitis 9.7
1970 herpes zoster ophthalmicus 9.7
1971 hydroa vacciniforme 9.7
1972 hyperacusis 9.7
1973 idiopathic edema 9.7
1974 idiopathic neutropenia 9.7
1975 laryngeal papillomatosis 9.7
1976 lichen planus pigmentosus 9.7
1977 linear iga disease 9.7
1978 lipogranulomatosis 9.7
1979 localized lipodystrophy 9.7
1980 lymphangiomatosis 9.7
1981 lymphomatoid granulomatosis 9.7
1982 lymphosarcoma 9.7
1983 mannose-binding lectin protein deficiency 9.7
1984 marchiafava bignami disease 9.7
1985 mollaret meningitis 9.7
1986 mycetoma 9.7
1987 mycobacterium marinum 9.7
1988 mycobacterium xenopi 9.7
1989 n acetyltransferase deficiency 9.7
1990 necrotizing autoimmune myopathy 9.7
1991 neurosyphilis 9.7
1992 nontuberculous mycobacterial lung disease 9.7
1993 ovarian epithelial cancer 9.7
1994 paraneoplastic cerebellar degeneration 9.7
1995 pasteurella multocida infection 9.7
1996 phocomelia 9.7
1997 polyarticular onset juvenile idiopathic arthritis 9.7
1998 properdin deficiency 9.7
1999 pyogenic granuloma 9.7
2000 quinquaud folliculitis decalvans 9.7
2001 remitting seronegative symmetrical synovitis with pitting edema 9.7
2002 retroperitoneal liposarcoma 9.7
2003 scleromyxedema 9.7
2004 serpiginous choroiditis 9.7
2005 slc4a1-associated distal renal tubular acidosis 9.7
2006 streptococcal group a invasive disease 9.7
2007 susac syndrome 9.7
2008 t-cell/histiocyte rich large b cell lymphoma 9.7
2009 thiopurine s methyltranferase deficiency 9.7
2010 tièche-jadassohn nevus 9.7
2011 trochleitis 9.7
2012 ulcerative proctitis 9.7
2013 virus associated hemophagocytic syndrome 9.7
2014 wallerian degeneration 9.7
2015 wells syndrome 9.7
2016 sporadic hemiplegic migraine 9.7
2017 anoxia 9.7
2018 central cord syndrome 9.7
2019 cerebral hypoxia 9.7
2020 dementia - subcortical 9.7
2021 extrapontine myelinolysis 9.7
2022 hypertonia 9.7
2023 hypotonia 9.7
2024 hypoxia 9.7
2025 meningitis and encephalitis 9.7
2026 mucopolysaccharidoses 9.7
2027 myoclonus 9.7
2028 traumatic brain injury 9.7
2029 whiplash 9.7
2030 primary cutaneous marginal zone b-cell lymphoma 9.7
2031 undifferentiated embryonal sarcoma of the liver 9.7
2032 b-cell non-hodgkin lymphoma 9.7
2033 rare systemic disease 9.7
2034 atrial standstill 9.7
2035 idiopathic acute transverse myelitis 9.7
2036 low-flow priapism 9.7
2037 hemophagocytic syndrome associated with an infection 9.7
2038 indeterminate cell histiocytosis 9.7
2039 primary hemophagocytic lymphohistiocytosis 9.7
2040 overlapping connective tissue disease 9.7
2041 chronic acquired demyelinating polyneuropathy 9.7
2042 herpetiform pemphigus 9.7
2043 temporomandibular joint anomaly 9.7
2044 rare lymphatic malformation 9.7
2045 primary cutaneous lymphoma 9.7
2046 autoimmune polyendocrinopathy type 4 9.7
2047 toxic oil syndrome 9.7
2048 acquired cutis laxa 9.7
2049 acute sensory ataxic neuropathy 9.7
2050 pharyngeal-cervical-brachial variant of guillain-barre syndrome 9.7
2051 variant abeta2m amyloidosis 9.7
2052 hydroa vacciniforme-like lymphoma 9.7
2053 phalangeal microgeodic syndrome 9.7
2054 diffuse palmoplantar keratoderma 9.7
2055 diffuse large b-cell lymphoma of the central nervous system 9.7
2056 acquired methemoglobinemia 9.7
2057 acquired cystic disease-associated renal cell carcinoma 9.7
2058 transient neonatal myasthenia gravis 9.7
2059 juvenile myasthenia gravis 9.7
2060 osteonecrosis of the jaw 9.7
2061 acute macular neuroretinopathy 9.7
2062 benign idiopathic neonatal seizures 9.7
2063 pneumococcal meningitis 9.7
2064 methotrexate toxicity 9.7
2065 bickerstaff brainstem encephalitis 9.7
2066 cancer-associated retinopathy 9.7
2067 rare genetic skin disease 9.7
2068 mixed-type autoimmune hemolytic anemia 9.7
2069 secondary intestinal lymphangiectasia 9.7
2070 transient pseudohypoaldosteronism 9.7
2071 hepatosplenic t-cell lymphoma 9.7
2072 infectious encephalitis 9.7
2073 primary hypophysitis 9.7
2074 primary bone dysplasia with increased bone density 9.7
2075 intravascular large b-cell lymphoma 9.7
2076 vitreoretinopathy 9.7
2077 primary adrenal insufficiency 9.7
2078 aregenerative anemia 9.7
2079 precursor t-cell acute lymphoblastic leukemia 9.7
2080 hydrops fetalis, nonimmune 9.7
2081 lymph node tuberculosis 9.7
2082 granulomatous rosacea 9.7
2083 iga nephropathy 1 9.6
2084 gaucher disease, type i 9.6
2085 splenic marginal zone lymphoma 9.6
2086 prostatitis 9.6
2087 essential thrombocythemia 9.6
2088 hairy cell leukemia 9.6
2089 facial dermatosis 9.6
2090 tertiary syphilis 9.6
2091 chorea, benign hereditary 9.6
2092 frontonasal dysplasia 1 9.6
2093 glycoprotein, renal 9.6
2094 chromosome 5q deletion syndrome 9.6
2095 pelger-huet anomaly 9.6
2096 popliteal cyst 9.6
2097 abetalipoproteinemia 9.6
2098 anemia, congenital dyserythropoietic, type ia 9.6
2099 reticuloendotheliosis, x-linked 9.6
2100 cyclic vomiting syndrome 9.6
2101 xanthomatosis 9.6
2102 chondrodysplasia punctata, brachytelephalangic, autosomal 9.6
2103 retinal cone dystrophy 4 9.6
2104 leber congenital amaurosis 10 9.6
2105 multiple sclerosis 2 9.6
2106 bartonellosis 9.6
2107 hepatorenal syndrome 9.6
2108 dysthymic disorder 9.6
2109 cough variant asthma 9.6
2110 congenital dyserythropoietic anemia 9.6
2111 neurogenic bowel 9.6
2112 multiple cranial nerve palsy 9.6
2113 plasmodium falciparum malaria 9.6
2114 methylmalonic acidemia 9.6
2115 gaucher's disease 9.6
2116 hereditary spastic paraplegia 9.6
2117 myoma 9.6
2118 lactic acidosis 9.6
2119 acute hemorrhagic encephalitis 9.6
2120 cleft lip 9.6
2121 isolated methylmalonic acidemia 9.6
2122 basaloid follicular hamartoma 9.6
2123 kienbock's disease 9.6
2124 nonseminomatous germ cell tumor 9.6
2125 pustulosis palmaris et plantaris 9.6
2126 rheumatoid vasculitis 9.6
2127 cleft lip/palate 9.6
2128 autoimmune hemolytic anemia, cold type 9.6
2129 granulomatous mastitis 9.6
2130 factor v deficiency 9.5
2131 factor vii deficiency 9.5
2132 lambert syndrome 9.5
2133 smith-lemli-opitz syndrome 9.5
2134 mental retardation, skeletal dysplasia, and abducens palsy 9.5
2135 west nile virus 9.5
2136 sting-associated vasculopathy, infantile-onset 9.5
2137 lymphoplasmacytic lymphoma 9.5
2138 ileocolitis 9.5
2139 keratoconus 9.5
2140 lymphocytic choriomeningitis 9.5
2141 oligohydramnios 9.5
2142 echinococcosis 9.5
2143 cholera 9.5
2144 neuroendocrine tumor 9.5
2145 gastric dilatation 9.5
2146 middle cerebral artery infarction 9.5
2147 ulnar neuropathy 9.5
2148 granular cell carcinoma 9.5
2149 elephantiasis 9.5
2150 pulmonary neuroendocrine tumor 9.5
2151 duodenitis 9.5
2152 upper respiratory tract disease 9.5
2153 congenital syphilis 9.5
2154 bap1 tumor predisposition syndrome 9.5
2155 immunotactoid glomerulopathy 9.5
2156 myotonia 9.5
2157 acute generalized exanthematous pustulosis 9.5
2158 igg4-related kidney disease 9.5
2159 prune belly syndrome 9.4
2160 coarctation of aorta 9.4
2161 esophageal cancer 9.4
2162 factor viii deficiency 9.4
2163 immunoglobulin e concentration, serum 9.4
2164 paramyotonia congenita of von eulenburg 9.4
2165 patterson pseudoleprechaunism syndrome 9.4
2166 polykaryocytosis inducer 9.4
2167 peutz-jeghers syndrome 9.4
2168 storm syndrome 9.4
2169 syringomyelia, noncommunicating isolated 9.4
2170 wilms tumor 1 9.4
2171 basal ganglia calcification, idiopathic, 1 9.4
2172 chondrosarcoma 9.4
2173 cystinuria 9.4
2174 ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia 9.4
2175 factor x deficiency 9.4
2176 hydrocephalus due to congenital stenosis of aqueduct of sylvius 9.4
2177 richards-rundle syndrome 9.4
2178 myeloperoxidase deficiency 9.4
2179 nephrotic syndrome, type 1 9.4
2180 osteoporosis, juvenile 9.4
2181 pulmonary alveolar microlithiasis 9.4
2182 refsum disease, classic 9.4
2183 wilson disease 9.4
2184 lubs x-linked mental retardation syndrome 9.4
2185 nephrotic syndrome, type 20 9.4
2186 arts syndrome 9.4
2187 hemophilia b 9.4
2188 oncocytoma 9.4
2189 nephrotic syndrome, type 2 9.4
2190 retinitis pigmentosa 18 9.4
2191 neuronal intranuclear inclusion disease 9.4
2192 hurler syndrome 9.4
2193 immunodeficiency, common variable, 1 9.4
2194 hypertension, diastolic 9.4
2195 complement factor h deficiency 9.4
2196 myd88 deficiency 9.4
2197 prekallikrein deficiency 9.4
2198 adiponectin, serum level of, quantitative trait locus 1 9.4
2199 aicardi-goutieres syndrome 5 9.4
2200 retinitis pigmentosa 55 9.4
2201 immunodeficiency, common variable, 8, with autoimmunity 9.4
2202 nephrotic syndrome, type 8 9.4
2203 autoimmune lymphoproliferative syndrome, type v 9.4
2204 nephrotic syndrome, type 13 9.4
2205 hypertrophic scars 9.4
2206 autoimmune uveitis 9.4
2207 pulmonary aspergilloma 9.4
2208 thelaziasis 9.4
2209 fusariosis 9.4
2210 congenital hypothyroidism 9.4
2211 hyperphosphatemia 9.4
2212 severe congenital neutropenia 9.4
2213 mantle cell lymphoma 9.4
2214 zollinger-ellison syndrome 9.4
2215 chronic venous insufficiency 9.4
2216 tonsil squamous cell carcinoma 9.4
2217 pain agnosia 9.4
2218 adenoid hypertrophy 9.4
2219 obstructive nephropathy 9.4
2220 coronavirus infectious disease 9.4
2221 benign teratoma 9.4
2222 familial glucocorticoid deficiency 9.4
2223 sting-associated vasculopathy with onset in infancy 9.4
2224 ehrlichiosis 9.4
2225 short bowel syndrome 9.4
2226 sphenoid sinusitis 9.4
2227 eastern equine encephalitis 9.4
2228 spastic quadriplegia 9.4
2229 myiasis 9.4
2230 pituitary apoplexy 9.4
2231 suppurative otitis media 9.4
2232 laryngostenosis 9.4
2233 tinea cruris 9.4
2234 detrusor sphincter dyssynergia 9.4
2235 biliary atresia 9.4
2236 chronic purulent otitis media 9.4
2237 cystic echinococcosis 9.4
2238 chronic cystitis 9.4
2239 disorders of sexual development 9.4
2240 exostosis 9.4
2241 myotonia congenita 9.4
2242 spondylosis 9.4
2243 leptospirosis 9.4
2244 orchitis 9.4
2245 granulomatous angiitis 9.4
2246 rhizomelic chondrodysplasia punctata 9.4
2247 cystic teratoma 9.4
2248 auditory system disease 9.4
2249 tic disorder 9.4
2250 skin squamous cell carcinoma 9.4
2251 lysosomal storage disease 9.4
2252 rhabdomyosarcoma 9.4
2253 syringomyelia 9.4
2254 angiomyolipoma 9.4
2255 carotid artery thrombosis 9.4
2256 plague 9.4
2257 placental site trophoblastic tumor 9.4
2258 ovary adenocarcinoma 9.4
2259 verrucous carcinoma 9.4
2260 trophoblastic neoplasm 9.4
2261 tick infestation 9.4
2262 persian gulf syndrome 9.4
2263 pulmonary blastoma 9.4
2264 embryoma 9.4
2265 bronchiolo-alveolar adenocarcinoma 9.4
2266 mature teratoma 9.4
2267 gastrinoma 9.4
2268 myxoid chondrosarcoma 9.4
2269 eosinophilic pneumonia 9.4
2270 acute stress disorder 9.4
2271 inherited metabolic disorder 9.4
2272 kimura disease 9.4
2273 monoclonal gammopathy of uncertain significance 9.4
2274 osteochondrosis 9.4
2275 kidney angiomyolipoma 9.4
2276 monocytic leukemia 9.4
2277 sezary's disease 9.4
2278 ritter's disease 9.4
2279 lymphangitis 9.4
2280 chronic dacryoadenitis 9.4
2281 yellow fever 9.4
2282 transient neonatal thrombocytopenia 9.4
2283 trichinosis 9.4