ADE
MCID: ACT049
MIFTS: 51

Acute Disseminated Encephalomyelitis (ADE)

Categories: Eye diseases, Infectious diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Acute Disseminated Encephalomyelitis

MalaCards integrated aliases for Acute Disseminated Encephalomyelitis:

Name: Acute Disseminated Encephalomyelitis 12 52 53 58 15 17
Acute Disseminated Encephalitis 12 58 71 32
Adem 12 52 58
Encephalomyelitis, Acute Disseminated 71
Encephalomyelitis Acute Disseminated 54
Ade 52

Characteristics:

Orphanet epidemiological data:

58
acute disseminated encephalomyelitis
Inheritance: Not applicable; Prevalence: 1-9/1000000 (Europe); Age of onset: All ages; Age of death: normal life expectancy;

Classifications:

Orphanet: 58  
Rare neurological diseases
Rare eye diseases


External Ids:

Disease Ontology 12 DOID:639
MeSH 43 D004673
NCIt 49 C34578
SNOMED-CT 67 83942000
ICD10 32 G04.0
ICD10 via Orphanet 33 G04.0
UMLS via Orphanet 72 C0014059
Orphanet 58 ORPHA83597
UMLS 71 C0014059 C3536864

Summaries for Acute Disseminated Encephalomyelitis

NINDS : 53 Acute disseminated encephalomyelitis (ADEM) is characterized by a brief but widespread attack of inflammation in the brain and spinal cord that damages myelin – the protective covering of nerve fibers.  ADEM often follows viral or bacterial infections, or less often, vaccination for measles, mumps, or rubella.  The symptoms of ADEM appear rapidly, beginning with encephalitis-like symptoms such as fever, fatigue, headache, nausea and vomiting, and in the most severe cases, seizures and coma.  ADEM typically damages white matter (brain tissue that takes its name from the white color of myelin), leading to neurological symptoms such as visual loss (due to inflammation of the optic nerve) in one or both eyes, weakness even to the point of paralysis, and difficulty coordinating voluntary muscle movements (such as those used in walking).  ADEM is sometimes misdiagnosed as a severe first attack of multiple sclerosis (MS), since the symptoms and the appearance of the white matter injury on brain imaging may be similar.  However, ADEM has several features which differentiate it from MS.  First, unlike MS patients, persons with ADEM will have rapid onset of fever, a history of recent infection or immunization, and some degree of impairment of consciousness, perhaps even coma; these features are not typically seen in MS.  Children are more likely than adults to have ADEM, whereas MS is a rare diagnosis in children.  In addition, ADEM usually consists of a single episode or attack of widespread myelin damage, while MS features many attacks over the course of time. Doctors will often use imaging techniques, such as MRI (magnetic resonance imaging), to search for old and new lesions (areas of damage) on the brain.  The presence of older brain lesions on MRI suggest that the condition may be MS rather than ADEM, since MS can cause brain lesions before symptoms become obvious.  In rare situations, a brain biopsy may be necessary to differentiate between ADEM and some other diseases that involve inflammation and damage to myelin.

MalaCards based summary : Acute Disseminated Encephalomyelitis, also known as acute disseminated encephalitis, is related to allergic encephalomyelitis and subacute sclerosing panencephalitis. An important gene associated with Acute Disseminated Encephalomyelitis is MBP (Myelin Basic Protein), and among its related pathways/superpathways are Innate Immune System and Cytokine Signaling in Immune system. The drugs Vaccines and Antibodies, Blocking have been mentioned in the context of this disorder. Affiliated tissues include brain, spinal cord and heart, and related phenotypes are hematopoietic system and immune system

Disease Ontology : 12 An encephalomyelitis characterized by inflammation locatedin brain and locatedin spinal cord that damages myelin. It usually occurs after viral infection, but also following vaccination, bacterial or parasitic infection.

NIH Rare Diseases : 52 Acute disseminated encephalomyelitis (ADEM) is a neurological condition characterized by a brief but intense attack of inflammation in the brain and spinal cord. This may lead to damage of the layer of insulation around the nerves (myelin ) within affected areas. ADEM often follows viral infection, or less often, vaccinations for measles, mumps, or rubella (MMR). Symptoms usually appear rapidly, beginning with fever, fatigue, headache, nausea and vomiting. Treatment for ADEM is targeted at suppressing inflammation in the brain using anti-inflammatory drugs. Most people begin to recover within days, with total or near-total recovery within a few months. Some people may have lifelong neurological impairments, and very rarely, severe cases can be fatal.

Wikipedia : 74 Acute disseminated encephalomyelitis (ADEM), or acute demyelinating encephalomyelitis, is a rare... more...

Related Diseases for Acute Disseminated Encephalomyelitis

Diseases related to Acute Disseminated Encephalomyelitis via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 1794, show less)
# Related Disease Score Top Affiliating Genes
1 allergic encephalomyelitis 33.5 MOG MBP
2 subacute sclerosing panencephalitis 33.3 MOG MBP IL10
3 dermatitis, atopic 31.8 MBP IL1B IL10 CD40LG CCR6 CCL4
4 chronic mucocutaneous candidiasis 31.7 IL1B IL10 CSF3 CCR6
5 pediatric multiple sclerosis 31.6 MOG HLA-DRB1 HLA-DQB1
6 transverse myelitis 31.3 MBP IL10 AQP4
7 mumps 31.1 IL10 HLA-DRB1 HLA-DQB1 CD40LG
8 measles 31.0 IL1B HLA-DRB1 HLA-DQA1 CD40LG
9 hypersomnia 31.0 HLA-DRB1 HLA-DQB1 HCRT
10 acute transverse myelitis 31.0 IL10 AQP4
11 chickenpox 30.9 IL10 CD40LG CCR6
12 aseptic meningitis 30.9 IL1B IL10 CSF3 CD40LG
13 meningoencephalitis 30.7 MBP IL10 CD40LG CCR6
14 quadriplegia 30.7 MOG MBP CCR6
15 appendicitis 30.6 IL1B IL10 CSF3
16 bacterial meningitis 30.6 IL1B IL10 CCL4 AQP4
17 neuritis 30.6 MPZ MOG MBP IL1B IL10 CCL4
18 brain edema 30.6 IL1B CSF3 AQP4
19 nervous system disease 30.6 MOG MBP IL1B CCR6
20 tetanus 30.5 MBP IL1B IL10 CD40LG
21 pharyngitis 30.5 IL1B HLA-DRB1 CD40LG
22 red cell aplasia 30.5 HLA-DRB1 HLA-DQB1 HLA-B
23 leptospirosis 30.5 IL1B IL10 HLA-DRB1 CD40LG
24 pneumonia 30.5 IL1B IL10 CSF3 CD40LG
25 gastroenteritis 30.5 IL1B IL10 CSF3
26 diarrhea 30.5 IL1B IL10 CSF3 CD40LG
27 herpes zoster 30.5 IL10 HLA-DRB1 HLA-B CD40LG
28 dengue disease 30.5 CD40LG CCR6 CCL4
29 brain injury 30.4 MBP IL10 AQP4
30 lupus erythematosus 30.4 IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 CD40LG
31 exanthem 30.4 IL10 CSF3 CD40LG CCR6
32 traumatic brain injury 30.4 MBP IL10 AQP4
33 acute cystitis 30.4 IL10 CD40LG CCR6
34 plasmodium falciparum malaria 30.4 IL10 CD40LG CCL4
35 acute retrobulbar neuritis 30.3 MBP AQP4
36 neuromyelitis optica 30.3 MOG MBP HLA-DRB1 HCRT CD40LG AQP4
37 balo concentric sclerosis 30.3 MOG MBP AQP4
38 polyneuropathy 30.3 MPZ MBP IL1B CD40LG
39 graft-versus-host disease 30.3 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-B
40 scrub typhus 30.3 IL1B IL10 CD40LG
41 cerebral palsy 30.3 IL1B IL10 CSF3
42 central nervous system vasculitis 30.3 HLA-DRB1 CD40LG CCR6
43 dengue shock syndrome 30.3 IL1B HLA-DRB1 CD40LG
44 duodenal ulcer 30.3 IL1B IL10 HLA-DRB1
45 osteomyelitis 30.2 IL1B IL10 CSF3
46 gingivitis 30.2 IL1B IL10 CSF3
47 sleep apnea 30.2 IL1B IL10 HCRT
48 chlamydia 30.2 IL1B IL10 CD40LG
49 internuclear ophthalmoplegia 30.2 MOG LGI1 AQP4
50 autoimmune encephalitis 30.2 LGI1 HCRT CNTNAP2
51 rubella 30.2 MOG IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1
52 pulmonary tuberculosis 30.2 IL10 HLA-DRB1 HLA-DQB1 CCL4
53 myositis 30.2 IL1B HLA-DRB1 HLA-DQA1 HLA-B
54 pure red-cell aplasia 30.2 HLA-DRB1 HLA-DQB1 HLA-B CD40LG
55 yellow fever 30.2 IL1B CD40LG CCR6
56 rheumatic fever 30.2 IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 CD40LG
57 central nervous system disease 30.2 MOG MBP IL1B HCRT CCR6
58 toxoplasmosis 30.1 IL1B IL10 HLA-DQB1 HLA-DQA1 CD40LG
59 dengue hemorrhagic fever 30.1 IL10 HLA-DRB1 HLA-B CD40LG
60 meningitis 30.1 IL1B IL10 HLA-B CSF3 CD40LG CCL4
61 stomatitis 30.1 IL1B IL10 CSF3 CD40LG
62 pulmonary edema 30.1 IL1B IL10 CSF3
63 pyelonephritis 30.1 IL1B IL10 CSF3
64 malaria 30.1 IL1B IL10 HLA-DRB1 HLA-B CSF3 CD40LG
65 sensory peripheral neuropathy 30.0 MPZ CSF3 CD40LG
66 toxic shock syndrome 30.0 IL1B IL10 CD40LG
67 intermediate uveitis 30.0 IL10 HLA-DRB1 HLA-B CCR6
68 combined t cell and b cell immunodeficiency 30.0 IL10 CD40LG CCR6
69 thrombocytopenic purpura, autoimmune 30.0 HLA-DRB1 CD40LG CCR6
70 adult respiratory distress syndrome 30.0 IL1B IL10 CSF3
71 endometritis 30.0 IL1B HLA-DQB1 HLA-DQA1
72 cholangitis 30.0 IL10 HLA-DRB1 HLA-B CD40LG
73 chronic inflammatory demyelinating polyradiculoneuropathy 29.9 MPZ MBP IL10 HLA-DRB1 CCL4
74 neurosarcoidosis 29.9 MOG DPYSL5 AQP4
75 crohn's disease 29.9 IL1B IL10 HLA-DRB1 CCR6
76 immune deficiency disease 29.9 IL10 HLA-B CD40LG CCR6 CCL4
77 guillain-barre syndrome 29.9 MPZ MOG MBP HLA-DRB1 HLA-DQB1 HLA-DQA1
78 myocarditis 29.9 IL1B IL10 HLA-DQB1 HLA-B CD40LG
79 perinatal necrotizing enterocolitis 29.9 IL1B IL10 CCR6
80 encephalitis 29.9 MOG LGI1 IL1B IL10 CNTNAP2 CD40LG
81 syphilis 29.8 HLA-DRB1 CD40LG CCR6
82 primary adrenal insufficiency 29.8 HLA-DRB1 HLA-DQB1 HLA-DQA1
83 graves' disease 29.8 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
84 relapsing polychondritis 29.8 IL10 CSF3 CCL4
85 von economo's disease 29.8 LGI1 HCRT CNTNAP2
86 ulcerative colitis 29.8 IL1B IL10 HLA-DRB1 CCR6
87 spondylitis 29.8 IL10 HLA-B CCR6
88 polyradiculoneuropathy 29.8 MPZ MBP IL10 HLA-DRB1 CD40LG CCL4
89 neuroretinitis 29.8 CD40LG AQP4
90 bacterial infectious disease 29.8 IL1B IL10 CSF3 CD40LG CCR6 CCL4
91 demyelinating disease 29.8 MPZ MOG MBP IL1B IL10 HLA-DRB1
92 invasive aspergillosis 29.7 IL10 CSF3 CCR6
93 colitis 29.7 IL1B IL10 HLA-DRB1 CCR6
94 lambert-eaton myasthenic syndrome 29.7 IL10 HLA-DQA1 HLA-B
95 lyme disease 29.7 IL1B HLA-DRB1 HLA-DQB1 CD40LG
96 cellulitis 29.7 IL10 CD40LG CCR6
97 myelitis 29.7 MOG MBP IL10 DPYSL5 CD40LG CCR6
98 keratitis, hereditary 29.7 IL1B IL10 CCR6
99 aspergillosis 29.7 IL1B IL10 CSF3 CCR6
100 typhoid fever 29.7 IL1B HLA-DRB1 HLA-DQB1 CD40LG CCR6
101 sclerosing cholangitis 29.7 IL10 HLA-DRB1 HLA-B CD40LG
102 cysticercosis 29.7 IL1B IL10 CD40LG
103 choreatic disease 29.6 LGI1 DPYSL5 CNTNAP2
104 spondyloarthropathy 29.6 IL1B IL10 HLA-B
105 dysentery 29.6 IL1B IL10 CD40LG CCR6
106 human immunodeficiency virus infectious disease 29.6 IL10 HLA-B CCR6 CCL4
107 pneumocystosis 29.6 CSF3 CD40LG CCR6
108 juvenile rheumatoid arthritis 29.6 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1
109 otitis media 29.6 IL1B IL10 CD40LG
110 optic neuritis 29.6 MPZ MOG MBP IL1B IL10 HLA-DRB1
111 calcinosis 29.6 HLA-DRB1 HLA-DQB1 HLA-DQA1
112 autoimmune hepatitis 29.5 IL10 HLA-DRB1 HLA-DQB1 CD40LG
113 rheumatic disease 29.5 IL1B IL10 HLA-DRB1 HLA-B CD40LG CCR6
114 myasthenia gravis 29.5 MBP IL10 HLA-DQB1 HLA-B
115 spondyloarthropathy 1 29.5 HLA-B CD40LG CCR6
116 pemphigus 29.5 IL10 HLA-DRB1 HLA-DQB1 CD40LG
117 kawasaki disease 29.5 IL1B IL10 CD40LG
118 viral encephalitis 29.5 MOG MBP LGI1 IL1B IL10 CD40LG
119 progressive multifocal leukoencephalopathy 29.5 MBP CD40LG CCR6
120 congenital toxoplasmosis 29.5 IL10 HLA-DQB1 HLA-DQA1 CD40LG
121 lymphoma, non-hodgkin, familial 29.5 IL10 HLA-DRB1 CSF3 CD40LG CCR6
122 leishmaniasis 29.5 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1
123 severe cutaneous adverse reaction 29.5 HLA-DRB1 HLA-DQB1 HLA-B CD40LG
124 secondary progressive multiple sclerosis 29.4 MBP IL10 CD40LG
125 leprosy 3 29.4 IL1B IL10 HLA-DRB1 HLA-DQA1 CD40LG CCR6
126 extrinsic allergic alveolitis 29.4 IL1B IL10 CCR6
127 salmonellosis 29.4 IL1B IL10 CCR6
128 hydrocephalus 29.4 MBP IL10 HCRT AQP4
129 viral hepatitis 29.4 IL10 HLA-DRB1 HLA-DQA1 CD40LG
130 narcolepsy 29.4 MOG HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B HCRT
131 mouth disease 29.3 IL1B IL10 CCR6 AQP4
132 bone inflammation disease 29.3 IL1B IL10 HLA-DRB1 CD40LG CCR6
133 parasitic helminthiasis infectious disease 29.3 IL10 CD40LG CCR6
134 aplastic anemia 29.3 IL1B IL10 HLA-DRB1 HLA-B CSF3
135 testicular disease 29.3 IL10 CD40LG CCR6
136 temporal arteritis 29.3 HLA-DRB1 CD40LG CCR6
137 pulmonary fibrosis, idiopathic 29.3 IL1B IL10 CCR6 CCL4
138 diabetes mellitus 29.2 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1
139 metachromatic leukodystrophy 29.2 MPZ MBP CDH23
140 bacterial pneumonia 29.2 IL10 CSF3 CD40LG CCR6
141 psoriatic arthritis 29.1 IL1B IL10 HLA-DRB1 HLA-B CD40LG CCR6
142 acquired immunodeficiency syndrome 29.1 MBP IL1B IL10 HLA-B CD40LG CCR6
143 sarcoidosis 1 29.1 IL1B HLA-DRB1 HLA-DQB1 CD40LG CCR6 CCL4
144 autoimmune disease 29.0 MOG MBP IL1B IL10 HLA-DRB1 HLA-DQB1
145 relapsing-remitting multiple sclerosis 29.0 MOG MBP IL1B IL10 HLA-DRB1 CD40LG
146 systemic lupus erythematosus 28.9 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1
147 multiple sclerosis 28.8 MPZ MOG MBP IL1B IL10 HLA-DRB1
148 arthritis 28.8 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
149 optic nerve disease 28.8 MOG MBP LGI1 DPYSL5 CD40LG CCR6
150 rheumatoid arthritis 28.8 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
151 stiff-person syndrome 28.7 LGI1 DPYSL5 CNTNAP2
152 primary biliary cirrhosis 28.7 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
153 celiac disease 1 28.7 IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1 HLA-B
154 schizophrenia 28.6 MOG MBP IL1B IL10 HLA-DRB1 HLA-DQB1
155 asthma 28.4 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1
156 inflammatory bowel disease 28.4 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1
157 diabetes mellitus, insulin-dependent 28.2 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
158 peripheral nervous system disease 28.2 MPZ MOG MBP IL1B IL10 DPYSL5
159 alzheimer disease 12.4
160 hyper-ige recurrent infection syndrome 1, autosomal dominant 12.1
161 acute hemorrhagic leukoencephalitis 11.9
162 immunodeficiency 27b 11.9
163 myopathy, centronuclear, 1 11.9
164 renal tubular acidosis, distal, autosomal dominant 11.8
165 postinfectious encephalomyelitis 11.8
166 hypocalcemia, autosomal dominant 1 11.7
167 early-onset, autosomal dominant alzheimer disease 11.7
168 alzheimer disease 2 11.7
169 anauxetic dysplasia 1 11.7
170 alcohol dependence 11.6
171 alzheimer disease 3 11.6
172 adenocarcinoma 11.5
173 striatonigral degeneration, infantile 11.5
174 acute flaccid myelitis 11.5
175 immune-mediated encephalomyelitis 11.5
176 frontotemporal lobar degeneration with tdp43 inclusions, grn-related 11.5
177 alzheimer disease 6 11.5
178 polycystic liver disease 11.5
179 frontotemporal dementia 11.4
180 alcohol use disorder 11.3
181 spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant 11.3
182 emery-dreifuss muscular dystrophy 7, autosomal dominant 11.3
183 rickets 11.3
184 parkinson disease, late-onset 11.3
185 posterior cortical atrophy 11.3
186 pick disease of brain 11.3
187 dementia, lewy body 11.3
188 keratomalacia 11.3
189 hypoascorbemia 11.3
190 churg-strauss syndrome 11.3
191 esophagitis, eosinophilic, 1 11.3
192 semantic dementia 11.3
193 epidermolysis bullosa dystrophica, autosomal dominant 11.2
194 familial mediterranean fever, autosomal dominant 11.2
195 palmoplantar keratoderma i, striate, focal, or diffuse 11.2
196 slowed nerve conduction velocity, autosomal dominant 11.2
197 mitochondrial dna depletion syndrome 12a , autosomal dominant 11.2
198 distal renal tubular acidosis 11.2
199 immunodeficiency 27a 11.1
200 hyper-ige recurrent infection syndrome 2, autosomal recessive 11.1
201 immunodeficiency 31a 11.1
202 brachyolmia 11.1
203 spinal muscular atrophy 11.1
204 ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant 11.1
205 otospondylomegaepiphyseal dysplasia, autosomal dominant 11.1
206 alzheimer disease mitochondrial 11.1
207 autosomal dominant spastic ataxia 11.1
208 autosomal dominant proximal renal tubular acidosis 11.1
209 anemia, congenital dyserythropoietic, type iii 11.0
210 heinz body anemias 11.0
211 parkinson disease 1, autosomal dominant 11.0
212 spinocerebellar ataxia 2 11.0
213 vasculopathy, retinal, with cerebral leukodystrophy 11.0
214 epidermolysis bullosa junctionalis with pyloric atresia 11.0
215 fanconi anemia, complementation group a 11.0
216 fructose intolerance, hereditary 11.0
217 spinal muscular atrophy, type i 11.0
218 spinal muscular atrophy, type ii 11.0
219 centronuclear myopathy 11.0
220 articulation disorder 11.0
221 gerstmann syndrome 11.0
222 chromosome 17q11.2 deletion syndrome 11.0
223 rohhad 11.0
224 encephalopathy 10.7
225 ataxia and polyneuropathy, adult-onset 10.7
226 limbic encephalitis with lgi1 antibodies 10.6 HLA-DRB1 HLA-DQB1
227 autoimmune polyglandular syndrome type 3 10.6 HLA-DRB1 HLA-DQB1
228 juvenile myasthenia gravis 10.6 IL10 HLA-DRB1
229 pain agnosia 10.6
230 ocular motor apraxia 10.6
231 type ii mixed cryoglobulinemia 10.6 HLA-DRB1 HLA-DQB1
232 postherpetic neuralgia 10.6 HLA-DRB1 HLA-B
233 achalasia, familial esophageal 10.6 HLA-DQB1 HLA-DQA1
234 recurrent respiratory papillomatosis 10.6 HLA-DRB1 HLA-DQB1
235 hypoglycemia 10.6
236 mesial temporal lobe epilepsy with hippocampal sclerosis 10.6 IL1B HLA-DRB1
237 dermatitis, atopic, 8 10.6 IL1B IL10
238 apple allergy 10.6 HLA-DRB1 HLA-DQB1
239 idiopathic hypersomnia 10.5 HLA-DQB1 HCRT
240 influenza 10.5
241 palladium allergic contact dermatitis 10.5 IL1B IL10
242 metal allergy 10.5 IL10 HLA-DRB1 HLA-DQB1
243 vascular myelopathy 10.5 MOG AQP4
244 moyamoya angiopathy 10.5 HLA-DRB1 HLA-DQB1 HLA-B
245 chronic beryllium disease 10.5 HLA-DRB1 HLA-DQB1 HLA-DPA1
246 kleine-levin hibernation syndrome 10.5 HLA-DQB1 HCRT
247 paraneoplastic pemphigus 10.5 HLA-DRB1 HLA-DQB1 HLA-B
248 alveolar echinococcosis 10.5 HLA-DRB1 HLA-DQB1 HLA-B
249 focal epithelial hyperplasia 10.5 HLA-DRB1 HLA-DQB1 HLA-DQA1
250 oligoarticular juvenile idiopathic arthritis 10.4 HLA-DRB1 HLA-DQB1 HLA-DQA1
251 narcolepsy 2 10.4 HLA-DRB1 HLA-DQB1 HCRT
252 cervical dystonia 10.4 HLA-DRB1 HLA-DQB1 HLA-DQA1
253 sympathetic ophthalmia 10.4 IL10 HLA-DRB1 HLA-DQA1
254 recurrent hypersomnia 10.4 HLA-DQB1 HCRT
255 osteosclerotic myeloma 10.4 IL1B CD40LG
256 aphasia 10.4
257 nontuberculous mycobacterial lung disease 10.4 HLA-DRB1 HLA-B
258 dementia 10.4
259 pathologic nystagmus 10.4
260 aphthous stomatitis 10.4 IL1B IL10 HLA-B
261 castleman disease 10.4 IL10 CSF3 CCL4
262 facial paralysis 10.4
263 visceral leishmaniasis 10.4 IL1B IL10 HLA-DRB1
264 actinic prurigo 10.4 IL1B HLA-DRB1
265 atrophic gastritis 10.3 IL1B IL10 HLA-DRB1
266 rabies 10.3
267 poliomyelitis 10.3
268 paraplegia 10.3
269 vasculitis 10.3
270 neuropathy 10.3
271 cytomegalovirus retinitis 10.3 IL10 HLA-DRB1 HLA-DQB1 HLA-B
272 autoimmune hepatitis type 1 10.3 IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1
273 autoimmune pancreatitis 10.3 IL10 HLA-DRB1 CD40LG
274 dermatitis 10.3
275 cryoglobulinemia 10.3 IL10 HLA-DRB1 CD40LG
276 japanese encephalitis 10.3
277 respiratory failure 10.3
278 herpes simplex 10.3
279 q fever 10.3 IL1B IL10 CD40LG
280 narcolepsy 1 10.3 MOG HLA-DRB1 HLA-DQB1 HCRT
281 meningovascular neurosyphilis 10.3 MBP CD40LG
282 idiopathic bronchiectasis 10.3 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
283 late congenital syphilis 10.3 CD40LG CCL4
284 beryllium disease 10.3 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-DPA1
285 optic papillitis 10.3 MOG CD40LG AQP4
286 aceruloplasminemia 10.3
287 hemiplegia 10.3
288 hepatitis a 10.3
289 headache 10.3
290 rheumatic heart disease 10.3 IL1B IL10 HLA-DRB1 HLA-DQA1
291 niemann-pick disease 10.3 MPZ MBP IL10
292 funisitis 10.3 IL1B IL10 CCR6
293 vaginitis 10.3 IL1B IL10 CCR6
294 neutropenia 10.2
295 gingival disease 10.2 IL1B IL10 CCR6
296 pars planitis 10.2 HLA-DRB1 HLA-B CCR6
297 acute chest syndrome 10.2 HLA-DRB1 HLA-DQB1 CSF3 CD40LG
298 hypercholesterolemia, familial, 1 10.2
299 congestive heart failure 10.2
300 rapidly involuting congenital hemangioma 10.2
301 lymphoma 10.2
302 mutism 10.2
303 vaginal disease 10.2 IL1B IL10 CCR6
304 depression 10.2
305 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.2
306 pityriasis rosea 10.2 HLA-DRB1 HLA-DQB1 HLA-B CD40LG
307 idiopathic neutropenia 10.2 IL1B IL10 HLA-DRB1 CD40LG
308 echinococcosis 10.2 IL10 HLA-DRB1 HLA-B CD40LG
309 dermatitis herpetiformis 10.2 IL10 HLA-DQB1 HLA-DQA1 CD40LG
310 cervical cancer 10.2
311 coronary heart disease 1 10.2
312 autoimmune polyendocrine syndrome 10.2 IL1B IL10 CCR6
313 heart disease 10.2
314 lipid metabolism disorder 10.2
315 ischemia 10.2
316 kearns-sayre syndrome 10.2
317 visual epilepsy 10.2
318 locked-in syndrome 10.2
319 plasmodium vivax malaria 10.2
320 squamous cell papilloma 10.2
321 papilloma 10.2
322 neuromyelitis optica spectrum disorder 10.2
323 cytomegalovirus infection 10.2
324 seizure disorder 10.2
325 tremor 10.2
326 takayasu arteritis 10.2 IL10 HLA-DRB1 HLA-B CD40LG
327 open-angle glaucoma 10.2
328 vascular dementia 10.2
329 mixed connective tissue disease 10.2 IL10 HLA-DRB1 HLA-DQA1 CD40LG
330 lung cancer 10.2
331 scoliosis 10.2
332 vascular disease 10.2
333 primary progressive multiple sclerosis 10.2 MOG MBP IL10 HLA-DRB1 HLA-DQB1
334 arteries, anomalies of 10.2
335 hyperlipoproteinemia, type iii 10.2
336 coronary artery anomaly 10.2
337 mental depression 10.2
338 immunoglobulin alpha deficiency 10.2 HLA-DQB1 CD40LG CCR6
339 peanut allergy 10.2 IL10 HLA-DRB1 HLA-DQB1 CCR6
340 lymphadenitis 10.2 IL1B IL10 CCR6
341 primary systemic mycosis 10.2 IL10 CD40LG CCR6
342 thrombocytopenia due to platelet alloimmunization 10.2 IL10 CD40LG CCR6
343 primary thrombocytopenia 10.2 IL10 CD40LG CCR6
344 amyloidosis 10.2
345 autoimmune disease of blood 10.2 IL10 CD40LG CCR6
346 vogt-koyanagi-harada disease 10.2 IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
347 dental caries 10.1
348 herpangina 10.1 IL10 CD40LG CCR6
349 splenic disease 10.1 IL10 CD40LG CCR6
350 retinal vasculitis 10.1 CD40LG CCR6 CCL4
351 kidney disease 10.1
352 osteoarthritis 10.1
353 48,xyyy 10.1
354 coccidiosis 10.1 IL10 CD40LG CCR6
355 autosomal dominant epilepsy with auditory features 10.1 LGI1 CNTNAP2
356 autoimmune disease of urogenital tract 10.1 IL10 CD40LG CCR6
357 hepatic vascular disease 10.1 CSF3 CD40LG CCR6
358 iritis 10.1 HLA-B CD40LG CCR6
359 chronic kidney disease 10.1
360 rectal disease 10.1 IL10 CD40LG CCR6
361 pfeiffer syndrome 10.1
362 myeloma, multiple 10.1
363 yemenite deaf-blind hypopigmentation syndrome 10.1
364 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.1
365 hydrops, lactic acidosis, and sideroblastic anemia 10.1
366 variola major 10.1
367 agraphia 10.1
368 common cold 10.1
369 leukodystrophy 10.1
370 pertussis 10.1
371 diphtheria 10.1
372 status epilepticus 10.1
373 dysgraphia 10.1
374 dystonia 10.1
375 smallpox 10.1
376 limbic encephalitis 10.1
377 hypotonia 10.1
378 myoclonus 10.1
379 infectious encephalitis 10.1
380 paranasal sinus disease 10.1 IL10 CD40LG CCR6
381 autism 10.1
382 pulmonary disease, chronic obstructive 10.1
383 adenoma 10.1
384 lymph node disease 10.1 IL10 CD40LG CCR6
385 b cell deficiency 10.1 IL10 CD40LG CCR6
386 nose disease 10.1 IL10 CD40LG CCR6
387 glaucoma, primary open angle 10.1
388 major depressive disorder 10.1
389 idiopathic scoliosis 10.1
390 pulmonary embolism 10.1
391 hypersensitivity reaction type iv disease 10.1 IL10 CD40LG CCR6
392 childhood type dermatomyositis 10.1 HLA-DQA1 CD40LG CCR6
393 atherosclerosis susceptibility 10.1
394 bladder cancer 10.1
395 triiodothyronine receptor auxiliary protein 10.1
396 atrial fibrillation 10.1
397 rectum cancer 10.1
398 corneal disease 10.1 IL1B IL10 CCR6
399 colorectal cancer 10.1
400 body mass index quantitative trait locus 1 10.1
401 constipation 10.1
402 hyperglycemia 10.1
403 reactive arthritis 10.1 IL1B IL10 HLA-B CCR6
404 stachybotrys chartarum 10.1 IL1B CCL4
405 cystic echinococcosis 10.1 IL10 HLA-DRB1 HLA-DQB1 HLA-B CD40LG
406 small cell cancer of the lung 10.1
407 methane production 10.1
408 pancreatic cancer 10.1
409 aging 10.1
410 lymphocytic leukemia 10.1
411 fatty liver disease 10.1
412 collagen disease 10.1 IL10 CD40LG CCR6
413 hepatocellular carcinoma 10.1
414 hypertension, essential 10.1
415 osteoporosis 10.1
416 ovarian cancer 10.1
417 scoliosis, isolated 1 10.1
418 anxiety 10.1
419 bone mineral density quantitative trait locus 8 10.1
420 bone mineral density quantitative trait locus 15 10.1
421 liver disease 10.1
422 chronic pain 10.1
423 pik3ca-related overgrowth syndrome 10.1
424 thyroid carcinoma 10.1
425 autism spectrum disorder 10.1
426 cerebellopontine angle meningioma 10.1 LGI1 DPYSL5
427 autoimmune neuropathy 10.1 MPZ CNTNAP2 CD40LG
428 blood coagulation disease 10.1 CSF3 CD40LG CCR6
429 prostate cancer 10.0
430 ocular hypertension 10.0
431 acute myocardial infarction 10.0
432 atrial standstill 1 10.0
433 attention deficit-hyperactivity disorder 10.0
434 hepatitis c virus 10.0
435 dengue virus 10.0
436 chorea, childhood-onset, with psychomotor retardation 10.0
437 chikungunya 10.0
438 zika fever 10.0
439 parotitis 10.0
440 viral meningitis 10.0
441 neurogenic bladder 10.0
442 common variable immunodeficiency 10.0
443 miller fisher syndrome 10.0
444 alexia 10.0
445 post-vaccinal encephalitis 10.0
446 hepatitis c 10.0
447 kluver-bucy syndrome 10.0
448 purpura 10.0
449 cerebritis 10.0
450 lactic acidosis 10.0
451 cranial nerve palsy 10.0
452 hemolytic anemia 10.0
453 gliomatosis cerebri 10.0
454 bronchitis 10.0
455 lymphopenia 10.0
456 axonal neuropathy 10.0
457 intracranial hypertension 10.0
458 47,xyy 10.0
459 cytokine deficiency 10.0
460 herpes simplex encephalitis 10.0
461 dysphagia 10.0
462 paresthesia 10.0
463 spasticity 10.0
464 specific language disorder 10.0
465 isolated optic neuritis 10.0
466 bickerstaff brainstem encephalitis 10.0
467 postinfectious encephalitis 10.0
468 lymphatic system disease 10.0 IL10 CD40LG CCR6
469 mucositis 10.0
470 rhinitis 10.0
471 opportunistic mycosis 10.0 IL10 CSF3 CD40LG CCR6
472 autoimmune disease of endocrine system 10.0 IL10 HLA-DRB1 CD40LG CCR6
473 hair disease 10.0 IL10 CSF3 CD40LG CCR6
474 hypertriglyceridemia, familial 10.0
475 angina pectoris 10.0
476 substance abuse 10.0
477 lacrimal apparatus disease 10.0 IL1B IL10 CD40LG CCR6
478 middle ear disease 10.0 IL1B IL10 CD40LG CCR6
479 conjunctival disease 10.0 IL1B IL10 CD40LG CCR6
480 dissociative amnesia 10.0 LGI1 CNTNAP2
481 extrinsic cardiomyopathy 10.0 IL1B IL10 CD40LG CCR6
482 commensal bacterial infectious disease 10.0 IL1B IL10 CD40LG CCR6
483 blood platelet disease 10.0 IL10 CSF3 CD40LG CCR6
484 pulmonary hypertension, primary, 1 10.0
485 down syndrome 10.0
486 human immunodeficiency virus type 1 10.0
487 myelodysplastic syndrome 10.0
488 liver cirrhosis 10.0
489 psoriasis 10.0
490 parasitic protozoa infectious disease 10.0 IL10 CD40LG CCR6
491 uveal disease 10.0 IL10 HLA-B CD40LG CCR6
492 bronchial disease 10.0 IL1B IL10 CD40LG CCR6
493 primary bacterial infectious disease 10.0 IL1B IL10 CD40LG CCR6
494 leukocyte disease 10.0 IL10 CSF3 CD40LG CCR6
495 allergic rhinitis 10.0
496 non-alcoholic fatty liver disease 10.0
497 pustulosis of palm and sole 10.0
498 b-cell lymphoma 10.0
499 lung disease 10.0
500 intermediate coronary syndrome 10.0
501 alopecia areata 10.0 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
502 hashimoto thyroiditis 10.0 IL1B IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 HLA-B
503 conduct disorder 10.0
504 hyperinsulinism 10.0
505 autoimmune gastritis 10.0 IL1B IL10 HLA-DRB1 HLA-B CCR6
506 amyotrophic lateral sclerosis 1 10.0
507 breast cancer 10.0
508 leukemia, chronic lymphocytic 10.0
509 nasopharyngeal carcinoma 10.0
510 intraocular pressure quantitative trait locus 10.0
511 microvascular complications of diabetes 3 10.0
512 microvascular complications of diabetes 4 10.0
513 microvascular complications of diabetes 6 10.0
514 microvascular complications of diabetes 7 10.0
515 diffuse large b-cell lymphoma 10.0
516 lateral sclerosis 10.0
517 skin disease 10.0
518 radiculopathy 10.0
519 fibromyalgia 10.0
520 podoconiosis 9.9 HLA-DQB1 HLA-DQA1
521 cystic fibrosis 9.9
522 endometrial cancer 9.9
523 myocardial infarction 9.9
524 microvascular complications of diabetes 5 9.9
525 pulmonary hypertension 9.9
526 bone resorption disease 9.9
527 pre-eclampsia 9.9
528 hyperparathyroidism 9.9
529 disease of mental health 9.9
530 melanoma 9.9
531 plague 9.9
532 eating disorder 9.9
533 in situ carcinoma 9.9
534 hansen's disease 9.9
535 head injury 9.9
536 autoimmune disease of musculoskeletal system 9.9 IL10 CD40LG CCR6
537 gastroesophageal reflux 9.9
538 creutzfeldt-jakob disease 9.9
539 diabetes mellitus, noninsulin-dependent 9.9
540 neural tube defects 9.9
541 tobacco addiction 9.9
542 body mass index quantitative trait locus 11 9.9
543 body mass index quantitative trait locus 9 9.9
544 macular degeneration, age-related, 1 9.9
545 body mass index quantitative trait locus 8 9.9
546 body mass index quantitative trait locus 4 9.9
547 body mass index quantitative trait locus 10 9.9
548 body mass index quantitative trait locus 7 9.9
549 smoking as a quantitative trait locus 3 9.9
550 body mass index quantitative trait locus 12 9.9
551 body mass index quantitative trait locus 14 9.9
552 fatty liver disease, nonalcoholic 1 9.9
553 body mass index quantitative trait locus 18 9.9
554 body mass index quantitative trait locus 19 9.9
555 body mass index quantitative trait locus 20 9.9
556 oppositional defiant disorder 9.9
557 mitral valve insufficiency 9.9
558 iron metabolism disease 9.9
559 infertility 9.9
560 schizoaffective disorder 9.9
561 adrenoleukodystrophy 9.9
562 chlamydia pneumonia 9.9
563 mitochondrial metabolism disease 9.9
564 adrenomyeloneuropathy 9.9
565 syncope 9.9
566 intracranial arteriosclerosis 9.9 LGI1 DPYSL5 AQP4
567 anisocoria 9.9
568 episodic kinesigenic dyskinesia 1 9.9
569 migraine with or without aura 1 9.9
570 obsessive-compulsive disorder 9.9
571 hypokalemic periodic paralysis, type 1 9.9
572 porphyria, acute intermittent 9.9
573 strabismus 9.9
574 thrombophilia due to thrombin defect 9.9
575 digeorge syndrome 9.9
576 torticollis 9.9
577 anemia, autoimmune hemolytic 9.9
578 lymphoma, hodgkin, classic 9.9
579 epilepsy, focal, with speech disorder and with or without mental retardation 9.9
580 melanosis, neurocutaneous 9.9
581 leigh syndrome 9.9
582 proteasome-associated autoinflammatory syndrome 1 9.9
583 rheumatic fever-related antigen 9.9
584 spastic pseudosclerosis 9.9
585 incontinentia pigmenti 9.9
586 mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes 9.9
587 stroke, ischemic 9.9
588 leukemia, acute myeloid 9.9
589 ventricular fibrillation, paroxysmal familial, 1 9.9
590 legionnaire disease 9.9
591 west nile virus 9.9
592 major affective disorder 8 9.9
593 major affective disorder 9 9.9
594 multiple sclerosis 3 9.9
595 early repolarization associated with ventricular fibrillation 9.9
596 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.9
597 striatal degeneration, autosomal dominant 2 9.9
598 deficiency anemia 9.9
599 west syndrome 9.9
600 streptococcus pneumonia 9.9
601 pemphigus gestationis 9.9
602 rocky mountain spotted fever 9.9
603 pontiac fever 9.9
604 aspiration pneumonia 9.9
605 swine influenza 9.9
606 epidemic typhus 9.9
607 lennox-gastaut syndrome 9.9
608 anaplastic large cell lymphoma 9.9
609 apraxia 9.9
610 visual agnosia 9.9
611 crohn's colitis 9.9
612 cardiac arrest 9.9
613 cryptococcal meningitis 9.9
614 hyper ige syndrome 9.9
615 sensorineural hearing loss 9.9
616 legionellosis 9.9
617 charcot-marie-tooth disease 9.9
618 eastern equine encephalitis 9.9
619 tooth disease 9.9
620 dissociative disorder 9.9
621 cholesteatoma of middle ear 9.9
622 pasteurellosis 9.9
623 spotted fever 9.9
624 choroiditis 9.9
625 horner's syndrome 9.9
626 oculomotor nerve paralysis 9.9
627 cauda equina syndrome 9.9
628 cortical blindness 9.9
629 allergic hypersensitivity disease 9.9
630 low compliance bladder 9.9
631 detrusor sphincter dyssynergia 9.9
632 acute leukemia 9.9
633 dilated cardiomyopathy 9.9
634 branch retinal artery occlusion 9.9
635 uveitis 9.9
636 porphyria 9.9
637 mycoplasma pneumoniae pneumonia 9.9
638 mixed malaria 9.9
639 neuroleptic malignant syndrome 9.9
640 pemphigoid gestationis 9.9
641 reye syndrome 9.9
642 papilledema 9.9
643 thrombocytopenia 9.9
644 conversion disorder 9.9
645 epilepsy 9.9
646 impotence 9.9
647 hepatitis b 9.9
648 psychotic disorder 9.9
649 landau-kleffner syndrome 9.9
650 agammaglobulinemia 9.9
651 glomerulonephritis 9.9
652 glioblastoma multiforme 9.9
653 central nervous system lymphoma 9.9
654 hyper ige recurrent infection syndrome 1 9.9
655 vaccinia 9.9
656 bipolar disorder 9.9
657 mood disorder 9.9
658 pleural empyema 9.9
659 agnosia 9.9
660 systemic scleroderma 9.9
661 myopathy 9.9
662 akinetic mutism 9.9
663 polyradiculopathy 9.9
664 seminoma 9.9
665 nominal aphasia 9.9
666 ideomotor apraxia 9.9
667 movement disease 9.9
668 demyelinating polyneuropathy 9.9
669 third cranial nerve disease 9.9
670 adenosine deaminase deficiency 9.9
671 cerebrovascular disease 9.9
672 mitochondrial myopathy 9.9
673 thyroiditis 9.9
674 muscular atrophy 9.9
675 neuroblastoma 9.9
676 end stage renal failure 9.9
677 localized scleroderma 9.9
678 retinal artery occlusion 9.9
679 bullous pemphigoid 9.9
680 malignant histiocytosis 9.9
681 subacute delirium 9.9
682 viral exanthem 9.9
683 myeloid leukemia 9.9
684 mitochondrial encephalomyopathy 9.9
685 learning disability 9.9
686 mechanical strabismus 9.9
687 toxocariasis 9.9
688 acute graft versus host disease 9.9
689 acute leukemia of ambiguous lineage 9.9
690 broken heart syndrome 9.9
691 central pain syndrome 9.9
692 chronic graft versus host disease 9.9
693 foix chavany marie syndrome 9.9
694 glioma 9.9
695 haemophilus influenzae 9.9
696 hhv-6 encephalitis 9.9
697 macrophage activation syndrome 9.9
698 mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes 9.9
699 pediatric acute-onset neuropsychiatric syndrome 9.9
700 pontine hemorrhage 9.9
701 primary central nervous system lymphoma 9.9
702 pseudobulbar affect 9.9
703 pure autonomic failure 9.9
704 spastic paraparesis 9.9
705 x-linked charcot-marie-tooth disease 9.9
706 aneurysm 9.9
707 back pain 9.9
708 hereditary neuropathies 9.9
709 hypertonia 9.9
710 spinal cord injury 9.9
711 glial tumor 9.9
712 periodic paralysis 9.9
713 pneumococcal meningitis 9.9
714 histiocytic sarcoma 9.9
715 rare surgical neurologic disease 9.9
716 chronic encephalitis 9.9
717 cardiogenic shock 9.9
718 acute motor axonal neuropathy 9.9
719 cerebral amyloid angiopathy, cst3-related 9.9
720 cardiac conduction defect 9.9
721 hair whorl 9.9
722 renal cell carcinoma, nonpapillary 9.9
723 insulin-like growth factor i 9.9
724 supranuclear palsy, progressive, 1 9.9
725 homocysteinemia 9.9
726 leukemia, acute lymphoblastic 9.9
727 cholangiocarcinoma 9.9
728 follicular lymphoma 9.9
729 pervasive developmental disorder 9.9
730 ductal carcinoma in situ 9.9
731 endocarditis 9.9
732 prostatic hypertrophy 9.9
733 primary hyperparathyroidism 9.9
734 bell's palsy 9.9
735 neuroendocrine tumor 9.9
736 enthesopathy 9.9
737 focal epilepsy 9.9
738 aortic aneurysm 9.9
739 intrahepatic cholangiocarcinoma 9.9
740 peritonitis 9.9
741 cervix uteri carcinoma in situ 9.9
742 alopecia 9.9
743 cervical intraepithelial neoplasia 9.9
744 autoimmune optic neuritis 9.9 MOG MBP DPYSL5 AQP4
745 osteogenic sarcoma 9.9
746 peripheral vascular disease 9.9
747 sexual disorder 9.9
748 inguinal hernia 9.9
749 glucose intolerance 9.9
750 polycystic ovary syndrome 9.9
751 gestational diabetes 9.9
752 gout 9.9
753 hemangioma 9.9
754 prostatic adenoma 9.9
755 severe combined immunodeficiency 9.9
756 achalasia 9.9
757 obsolete: squamous cell carcinoma of head and neck 9.9
758 esophageal cancer 9.8
759 fibrosis of extraocular muscles, congenital, 1 9.8
760 prostatic hyperplasia, benign 9.8
761 gallbladder disease 1 9.8
762 lung cancer susceptibility 3 9.8
763 gastric cancer 9.8
764 leukemia, acute lymphoblastic 3 9.8
765 helix syndrome 9.8
766 spastic cerebral palsy 9.8
767 withdrawal disorder 9.8
768 thrombosis 9.8
769 leukemia 9.8
770 eclampsia 9.8
771 hypothyroidism 9.8
772 cholera 9.8
773 squamous cell carcinoma 9.8
774 kidney cancer 9.8
775 benign mesothelioma 9.8
776 bilirubin metabolic disorder 9.8
777 tic disorder 9.8
778 newcastle disease 9.8
779 skin carcinoma 9.8
780 pancreatic ductal adenocarcinoma 9.8
781 conjunctivitis 9.8
782 periodontitis 9.8
783 allergic asthma 9.8
784 muscular dystrophy 9.8
785 hypereosinophilic syndrome 9.8
786 chromosomal triplication 9.8
787 ovarian epithelial cancer 9.8
788 histoplasmosis 9.8 HLA-DRB1 HLA-DQA1 HLA-B CD40LG CCR6
789 neurofibromatosis, type ii 9.8
790 scleroderma, familial progressive 9.8
791 suppressor of tumorigenicity 3 9.8
792 varicose veins 9.8
793 enterocolitis 9.8
794 sudden infant death syndrome 9.8
795 arts syndrome 9.8
796 barrett esophagus 9.8
797 tendinopathy 9.8
798 tendinitis 9.8
799 mantle cell lymphoma 9.8
800 metabolic acidosis 9.8
801 estrogen-receptor positive breast cancer 9.8
802 polycystic kidney disease 9.8
803 nasopharyngitis 9.8
804 sarcoma 9.8
805 esophagitis 9.8
806 hepatic coma 9.8
807 pyloric stenosis 9.8
808 hepatic encephalopathy 9.8
809 pneumothorax 9.8
810 acromegaly 9.8
811 idiopathic interstitial pneumonia 9.8
812 endometriosis 9.8
813 acute kidney failure 9.8
814 temporal lobe epilepsy 9.8
815 pulmonary fibrosis 9.8
816 gastritis 9.8
817 tricuspid valve insufficiency 9.8
818 spindle cell sarcoma 9.8
819 coronary stenosis 9.8
820 sleep disorder 9.8
821 panic disorder 9.8
822 spinal stenosis 9.8
823 cataract 9.8
824 polycythemia 9.8
825 skin melanoma 9.8
826 autosomal dominant polycystic kidney disease 9.8
827 corticobasal degeneration 9.8
828 posttransplant acute limbic encephalitis 9.8
829 rare disease in surgical orthopedic 9.8
830 panuveitis 9.7 IL10 HLA-DRB1 HLA-DQB1 HLA-B CD40LG CCR6
831 x-linked recessive disease 9.7 IL10 CD40LG CCR6
832 aortic aneurysm, familial abdominal, 1 9.7
833 hypercarotenemia and vitamin a deficiency, autosomal dominant 9.7
834 exudative vitreoretinopathy 1 9.7
835 thyroid carcinoma, familial medullary 9.7
836 papillomatosis, confluent and reticulated 9.7
837 pelvic organ prolapse 9.7
838 spastic paraplegia 4, autosomal dominant 9.7
839 hutterite cerebroosteonephrodysplasia syndrome 9.7
840 squamous cell carcinoma, head and neck 9.7
841 helicobacter pylori infection 9.7
842 branchiootic syndrome 1 9.7
843 anorexia nervosa 9.7
844 leukemia, chronic myeloid 9.7
845 hypophosphatemia 9.7
846 infective endocarditis 9.7
847 thalassemia 9.7
848 amnestic disorder 9.7
849 trachoma 9.7
850 myopia 9.7
851 dysthymic disorder 9.7
852 hypertrophic pyloric stenosis 9.7
853 carotid stenosis 9.7
854 patent foramen ovale 9.7
855 premature ejaculation 9.7
856 familial hypercholesterolemia 9.7
857 shoulder impingement syndrome 9.7
858 heart septal defect 9.7
859 islet cell tumor 9.7
860 cholecystitis 9.7
861 transient cerebral ischemia 9.7
862 ankylosis 9.7
863 thrombophilia 9.7
864 hereditary spastic paraplegia 9.7
865 basal cell carcinoma 9.7
866 opiate dependence 9.7
867 synovitis 9.7
868 acute pancreatitis 9.7
869 fibrosarcoma 9.7
870 pituitary adenoma 9.7
871 thyroid gland medullary carcinoma 9.7
872 heart valve disease 9.7
873 acute stress disorder 9.7
874 prion disease 9.7
875 anthrax disease 9.7
876 peptic ulcer disease 9.7
877 parathyroid adenoma 9.7
878 hyperthyroidism 9.7
879 rem sleep behavior disorder 9.7
880 croup 9.7
881 systolic heart failure 9.7
882 hypertrophic cardiomyopathy 9.7
883 oral cancer 9.7
884 polymyositis 9.7
885 soft tissue sarcoma 9.7
886 anoxia 9.7
887 virus-associated trichodysplasia spinulosa 9.7
888 autoimmune disease of gastrointestinal tract 9.7 IL10 HLA-DRB1 HLA-DQB1 HLA-DQA1 CD40LG CCR6
889 behcet syndrome 9.7 IL1B IL10 HLA-DRB1 HLA-B CD40LG CCR6
890 viral infectious disease 9.7 IL1B IL10 HLA-B CD40LG CCR6 CCL4
891 progressive familial heart block, type ia 9.7
892 burkitt lymphoma 9.7
893 carpal tunnel syndrome 9.7
894 hand skill, relative 9.7
895 pectus excavatum 9.7
896 pheochromocytoma 9.7
897 retinal detachment 9.7
898 retinoblastoma 9.7
899 schistosoma mansoni infection, susceptibility/ 9.7
900 vitiligo-associated multiple autoimmune disease susceptibility 6 9.7
901 chondrosarcoma 9.7
902 polycythemia vera 9.7
903 senile plaque formation 9.7
904 thymoma, familial 9.7
905 graves disease 1 9.7
906 vitiligo-associated multiple autoimmune disease susceptibility 1 9.7
907 gastrointestinal stromal tumor 9.7
908 bulimia nervosa 9.7
909 kala-azar 1 9.7
910 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.7
911 acute diarrhea 9.7
912 peripheral artery disease 9.7
913 oral squamous cell carcinoma 9.7
914 adrenal gland pheochromocytoma 9.7
915 non-alcoholic steatohepatitis 9.7
916 left bundle branch hemiblock 9.7
917 bubonic plague 9.7
918 spastic diplegia 9.7
919 hydronephrosis 9.7
920 anogenital venereal wart 9.7
921 hypoparathyroidism 9.7
922 infant gynecomastia 9.7
923 patau syndrome 9.7
924 inflammatory spondylopathy 9.7
925 goiter 9.7
926 alcoholic hepatitis 9.7
927 gynecomastia 9.7
928 hellp syndrome 9.7
929 color blindness 9.7
930 interstitial cystitis 9.7
931 schistosomiasis 9.7
932 generalized anxiety disorder 9.7
933 candidiasis 9.7
934 urticaria 9.7
935 normal pressure hydrocephalus 9.7
936 endogenous depression 9.7
937 cystitis 9.7
938 rectum adenocarcinoma 9.7
939 post-traumatic stress disorder 9.7
940 thrombocytosis 9.7
941 hepatitis 9.7
942 kernicterus 9.7
943 food allergy 9.7
944 rhabdomyosarcoma 9.7
945 thymoma 9.7
946 carotid artery disease 9.7
947 multidrug-resistant tuberculosis 9.7
948 pancreatic adenocarcinoma 9.7
949 dyslexia 9.7
950 macular retinal edema 9.7
951 avian influenza 9.7
952 hypokalemia 9.7
953 familial retinoblastoma 9.7
954 pancreatitis 9.7
955 malignant pleural mesothelioma 9.7
956 ileus 9.7
957 fascioliasis 9.7
958 fasciitis 9.7
959 substance dependence 9.7
960 sickle cell disease 9.7
961 spastic paraplegia 4 9.7
962 biliary tract cancer 9.7
963 bronchopulmonary dysplasia 9.7
964 granulocytopenia 9.7
965 pudendal neuralgia 9.7
966 bunion 9.7
967 cerebral atrophy 9.7
968 differentiated thyroid carcinoma 9.7
969 benign idiopathic neonatal seizures 9.7
970 obsolete: combined hyperlipidemia 9.7
971 connective tissue disease 9.7 IL1B IL10 HLA-DRB1 HLA-DQA1 CD40LG CCR6
972 apnea, obstructive sleep 9.6
973 machado-joseph disease 9.6
974 alopecia, androgenetic, 1 9.6
975 chiari malformation type i 9.6
976 dentatorubral-pallidoluysian atrophy 9.6
977 erythroleukemia, familial 9.6
978 hernia, hiatus 9.6
979 ige responsiveness, atopic 9.6
980 intussusception 9.6
981 marfan syndrome 9.6
982 medulloblastoma 9.6
983 melanoma, uveal 9.6
984 exfoliation syndrome 9.6
985 spondylolisthesis 9.6
986 thrombocytopenia 2 9.6
987 thyroid cancer, nonmedullary, 1 9.6
988 wolff-parkinson-white syndrome 9.6
989 acrocallosal syndrome 9.6
990 alexander disease 9.6
991 chordoma 9.6
992 galactorrhea 9.6
993 moyamoya disease 1 9.6
994 myelofibrosis 9.6
995 pancreatic agenesis 1 9.6
996 retinitis pigmentosa 9.6
997 tardive dyskinesia 9.6
998 uruguay faciocardiomusculoskeletal syndrome 9.6
999 oncocytoma 9.6
1000 adenomyosis 9.6
1001 suppression of tumorigenicity 12 9.6
1002 astigmatism 9.6
1003 microvascular complications of diabetes 1 9.6
1004 ascaris lumbricoides infection 9.6
1005 reflex sympathetic dystrophy 9.6
1006 late-onset retinal degeneration 9.6
1007 meningioma, radiation-induced 9.6
1008 atrioventricular septal defect 9.6
1009 spermatogenic failure 3 9.6
1010 meningioma, familial 9.6
1011 resting heart rate, variation in 9.6
1012 ovarian cancer 1 9.6
1013 ovarian hyperstimulation syndrome 9.6
1014 hypertension, diastolic 9.6
1015 microphthalmia, syndromic 10 9.6
1016 acute promyelocytic leukemia 9.6
1017 microvascular complications of diabetes 2 9.6
1018 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.6
1019 hearing loss, noise-induced 9.6
1020 aortic valve disease 2 9.6
1021 alacrima, achalasia, and mental retardation syndrome 9.6
1022 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 9.6
1023 gastrointestinal ulceration, recurrent, with dysfunctional platelets 9.6
1024 hypertrophic scars 9.6
1025 hyperphosphatemia 9.6
1026 fetal alcohol syndrome 9.6
1027 fetal alcohol spectrum disorder 9.6
1028 autosomal recessive disease 9.6
1029 paraganglioma 9.6
1030 androgenic alopecia 9.6
1031 atrioventricular block 9.6
1032 diabetic encephalopathy 9.6
1033 colorectal adenocarcinoma 9.6
1034 hepatocellular adenoma 9.6
1035 anosognosia 9.6
1036 generalized epilepsy with febrile seizures plus 9.6
1037 glucocorticoid-induced osteoporosis 9.6
1038 pollen allergy 9.6
1039 bone disease 9.6
1040 childhood acute lymphocytic leukemia 9.6
1041 adenoid cystic carcinoma 9.6
1042 hypogonadotropic hypogonadism 9.6
1043 osteonecrosis 9.6
1044 dermatomyositis 9.6
1045 pneumoconiosis 9.6
1046 anthracosis 9.6
1047 suppression amblyopia 9.6
1048 amblyopia 9.6
1049 esophageal atresia 9.6
1050 microinvasive gastric cancer 9.6
1051 short bowel syndrome 9.6
1052 portal hypertension 9.6
1053 ovarian disease 9.6
1054 brucellosis 9.6
1055 pulpitis 9.6
1056 disseminated intravascular coagulation 9.6
1057 arteriovenous malformation 9.6
1058 schizophreniform disorder 9.6
1059 spinal meningioma 9.6
1060 hemopericardium 9.6
1061 autonomic neuropathy 9.6
1062 penile cancer 9.6
1063 portal vein thrombosis 9.6
1064 emery-dreifuss muscular dystrophy 9.6
1065 iron deficiency anemia 9.6
1066 pericardial effusion 9.6
1067 protein-energy malnutrition 9.6
1068 nephrotic syndrome 9.6
1069 denture stomatitis 9.6
1070 cryptococcosis 9.6
1071 male infertility 9.6
1072 leiomyoma 9.6
1073 telangiectasis 9.6
1074 hypercementosis 9.6
1075 focal segmental glomerulosclerosis 9.6
1076 background diabetic retinopathy 9.6
1077 cholestasis 9.6
1078 obstructive jaundice 9.6
1079 dental fluorosis 9.6
1080 peptic esophagitis 9.6
1081 algoneurodystrophy 9.6
1082 anus cancer 9.6
1083 frozen shoulder 9.6
1084 acute cholangitis 9.6
1085 patellofemoral pain syndrome 9.6
1086 autosomal dominant cerebellar ataxia 9.6
1087 angioedema 9.6
1088 neuroendocrine carcinoma 9.6
1089 hyperuricemia 9.6
1090 hypogonadism 9.6
1091 exostosis 9.6
1092 hyperostosis 9.6
1093 enamel erosion 9.6
1094 extratemporal epilepsy 9.6
1095 larynx cancer 9.6
1096 pancreas disease 9.6
1097 chondroma 9.6
1098 glycogen storage disease 9.6
1099 contact dermatitis 9.6
1100 nonspecific interstitial pneumonia 9.6
1101 acquired polycythemia 9.6
1102 bronchiolitis 9.6
1103 iga glomerulonephritis 9.6
1104 allergic contact dermatitis 9.6
1105 malignant glioma 9.6
1106 interstitial lung disease 9.6
1107 ascaridiasis 9.6
1108 oligodendroglioma 9.6
1109 complex regional pain syndrome 9.6
1110 teratoma 9.6
1111 liposarcoma 9.6
1112 histiocytosis 9.6
1113 breast adenocarcinoma 9.6
1114 choriocarcinoma 9.6
1115 retinitis 9.6
1116 wheat allergy 9.6
1117 olfactory neuroblastoma 9.6
1118 anovulation 9.6
1119 lynch syndrome 9.6
1120 acute myocarditis 9.6
1121 thyroid gland papillary carcinoma 9.6
1122 myofascial pain syndrome 9.6
1123 ebola hemorrhagic fever 9.6
1124 hepatitis e 9.6
1125 chromophobe renal cell carcinoma 9.6
1126 secretory meningioma 9.6
1127 lymphoplasmacyte-rich meningioma 9.6
1128 bile duct cancer 9.6
1129 uremia 9.6
1130 essential tremor 9.6
1131 arteriolosclerosis 9.6
1132 aortic disease 9.6
1133 intestinal disease 9.6
1134 silent myocardial infarction 9.6
1135 inherited metabolic disorder 9.6
1136 hypogonadotropism 9.6
1137 diverticulitis 9.6
1138 cocaine abuse 9.6
1139 septic arthritis 9.6
1140 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.6
1141 oropharynx cancer 9.6
1142 tongue cancer 9.6
1143 degenerative disc disease 9.6
1144 mucocutaneous leishmaniasis 9.6
1145 diabetic macular edema 9.6
1146 central sleep apnea 9.6
1147 homocystinuria 9.6
1148 cleft lip 9.6
1149 keratoconjunctivitis 9.6
1150 postpartum depression 9.6
1151 pulmonary emphysema 9.6
1152 drug dependence 9.6
1153 cocaine dependence 9.6
1154 hemophilia 9.6
1155 ankrd26-related thrombocytopenia 9.6
1156 genetic prion diseases 9.6
1157 al amyloidosis 9.6
1158 anaplastic oligoastrocytoma 9.6
1159 brain tumor, childhood 9.6
1160 chiari malformation 9.6
1161 chronic thromboembolic pulmonary hypertension 9.6
1162 congenital rubella 9.6
1163 dentinogenesis imperfecta type 2 9.6
1164 enchondroma 9.6
1165 microscopic polyangiitis 9.6
1166 splenomegaly 9.6
1167 stevens-johnson syndrome/toxic epidermal necrolysis 9.6
1168 sudden sensorineural hearing loss 9.6
1169 true thymic hyperplasia 9.6
1170 color vision deficiency 9.6
1171 hypoxia 9.6
1172 obsolete: atypical teratoid/rhabdoid tumor 9.6
1173 malignant tumor of penis 9.6
1174 lysosomal disease 9.6
1175 rare tumor 9.6
1176 dementia pugilistica 9.6
1177 overgrowth syndrome 9.6
1178 hyperekplexia 9.5 LGI1 DPYSL5 CNTNAP2
1179 la crosse encephalitis 9.5 LGI1 DPYSL5 CNTNAP2 CD40LG
1180 immune system disease 9.4 MOG MBP IL1B IL10 CD40LG CCR6
1181 alacrima, congenital, autosomal dominant 9.4
1182 total anomalous pulmonary venous return 1 9.4
1183 sveinsson chorioretinal atrophy 9.4
1184 aortic valve disease 1 9.4
1185 blue rubber bleb nevus 9.4
1186 caffey disease 9.4
1187 carcinoid tumors, intestinal 9.4
1188 cleft palate, isolated 9.4
1189 cone-rod dystrophy 2 9.4
1190 cornea plana 1, autosomal dominant 9.4
1191 craniofacial-deafness-hand syndrome 9.4
1192 major affective disorder 1 9.4
1193 dystonia, dopa-responsive 9.4
1194 factor viii deficiency 9.4
1195 floating-harbor syndrome 9.4
1196 gilles de la tourette syndrome 9.4
1197 glioma susceptibility 1 9.4
1198 diaphragmatic hernia, congenital 9.4
1199 huntington disease 9.4
1200 hyperlipoproteinemia, type v 9.4
1201 hypogonadotropic hypogonadism 7 with or without anosmia 9.4
1202 multiple system atrophy 1 9.4
1203 inclusion body myositis 9.4
1204 kabuki syndrome 1 9.4
1205 lentigines 9.4
1206 macular dystrophy, vitelliform, 2 9.4
1207 meralgia paraesthetica, familial 9.4
1208 mesothelioma, malignant 9.4
1209 metaphyseal chondrodysplasia, schmid type 9.4
1210 motion sickness 9.4
1211 facioscapulohumeral muscular dystrophy 1 9.4
1212 facioscapulohumeral muscular dystrophy 2 9.4
1213 night blindness, congenital stationary, autosomal dominant 2 9.4
1214 nephrolithiasis, calcium oxalate 9.4
1215 pernicious anemia 9.4
1216 platelet membrane fluidity 9.4
1217 polykaryocytosis inducer 9.4
1218 familial adenomatous polyposis 1 9.4
1219 protoporphyria, erythropoietic, 1 9.4
1220 dowling-degos disease 1 9.4
1221 silver-russell syndrome 9.4
1222 emery-dreifuss muscular dystrophy 2, autosomal dominant 9.4
1223 spastic paraplegia 3, autosomal dominant 9.4
1224 chromosome 2q35 duplication syndrome 9.4
1225 syringomyelia, noncommunicating isolated 9.4
1226 tarsal coalition 9.4
1227 testicular torsion 9.4
1228 tetralogy of fallot 9.4
1229 thrombophilia due to activated protein c resistance 9.4
1230 trigeminal neuralgia 9.4
1231 tuberous sclerosis 1 9.4
1232 vesicoureteral reflux 1 9.4
1233 vitreoretinopathy, neovascular inflammatory 9.4
1234 volvulus of midgut 9.4
1235 wilms tumor 1 9.4
1236 acrodermatitis enteropathica, zinc-deficiency type 9.4
1237 acyl-coa dehydrogenase, short-chain, deficiency of 9.4
1238 adrenocortical carcinoma, hereditary 9.4
1239 anencephaly 9.4
1240 anus, imperforate 9.4
1241 australia antigen 9.4
1242 chediak-higashi syndrome 9.4
1243 charge syndrome 9.4
1244 plasminogen deficiency, type i 9.4
1245 fraser syndrome 1 9.4
1246 factor x deficiency 9.4
1247 glycogen storage disease ii 9.4
1248 hemochromatosis, type 1 9.4
1249 hydrocephalus, congenital, 1 9.4
1250 richards-rundle syndrome 9.4
1251 plasmodium falciparum blood infection level 9.4
1252 maple syrup urine disease 9.4
1253 mucopolysaccharidosis, type iiic 9.4
1254 mycosis fungoides 9.4
1255 epilepsy, myoclonic juvenile 9.4
1256 3-methylglutaconic aciduria, type iii 9.4
1257 nonarteritic anterior ischemic optic neuropathy 9.4
1258 osteoid osteoma 9.4
1259 abnormal hair, joint laxity, and developmental delay 9.4
1260 pseudoxanthoma elasticum 9.4
1261 pulmonary alveolar microlithiasis 9.4
1262 tay-sachs disease 9.4
1263 testicular germ cell tumor 9.4
1264 dihydropyrimidine dehydrogenase deficiency 9.4
1265 alopecia, congenital 9.4
1266 x inactivation, familial skewed, 1 9.4
1267 fabry disease 9.4
1268 hemophilia a 9.4
1269 congenital hemidysplasia with ichthyosiform erythroderma and limb defects 9.4
1270 premature ovarian failure 1 9.4
1271 tarp syndrome 9.4
1272 retinitis pigmentosa-deafness syndrome 9.4
1273 fatal familial insomnia 9.4
1274 short tarsus with absence of lower eyelashes 9.4
1275 epilepsy, idiopathic generalized 9.4
1276 fryns microphthalmia syndrome 9.4
1277 budd-chiari syndrome 9.4
1278 amelia, posterior, with pelvic and pulmonary hypoplasia syndrome 9.4
1279 patent ductus venosus 9.4
1280 cataract 3, multiple types 9.4
1281 wilms tumor 5 9.4
1282 trichothiodystrophy 1, photosensitive 9.4
1283 xanthomatosis 9.4
1284 schizophrenia 2 9.4
1285 hemophagocytic lymphohistiocytosis, familial, 2 9.4
1286 polydactyly 9.4
1287 intervertebral disc disease 9.4
1288 alpha-thalassemia 9.4
1289 chudley-mccullough syndrome 9.4
1290 epilepsy, familial focal, with variable foci 1 9.4
1291 progressive familial heart block, type ib 9.4
1292 orthostatic intolerance 9.4
1293 huntington disease-like 3 9.4
1294 langerhans cell histiocytosis 9.4
1295 north american indian childhood cirrhosis 9.4
1296 abdominal obesity-metabolic syndrome 1 9.4
1297 huntington disease-like 2 9.4
1298 glaucoma, normal tension 9.4
1299 alzheimer disease 4 9.4
1300 creatinine clearance quantitative trait locus 9.4
1301 angioid streaks 9.4
1302 spastic paraplegia 7, autosomal recessive 9.4
1303 mammographic density 9.4
1304 patent ductus arteriosus 1 9.4
1305 parathyroid carcinoma 9.4
1306 granulomatosis with polyangiitis 9.4
1307 pseudohyperkalemia, familial, 2, due to red cell leak 9.4
1308 hyperinsulinemic hypoglycemia, familial, 5 9.4
1309 hyperinsulinemic hypoglycemia, familial, 4 9.4
1310 immunodeficiency 25 9.4
1311 kleefstra syndrome 1 9.4
1312 preterm premature rupture of the membranes 9.4
1313 chromosome 16p13.3 deletion syndrome, proximal 9.4
1314 asthma-related traits 4 9.4
1315 thrombocytopenia 4 9.4
1316 ewing sarcoma 9.4
1317 diabetes mellitus, ketosis-prone 9.4
1318 chromosome 2p16.1-p15 deletion syndrome 9.4
1319 pancreatic cancer 3 9.4
1320 myxoid liposarcoma 9.4
1321 ectodermal dysplasia-syndactyly syndrome 2 9.4
1322 cholangitis, primary sclerosing 9.4
1323 cyanosis, transient neonatal 9.4
1324 fanconi anemia, complementation group l 9.4
1325 hypertelorism, preauricular sinus, punctal pits, and deafness 9.4
1326 microcephaly, epilepsy, and diabetes syndrome 9.4
1327 rigidity and multifocal seizure syndrome, lethal neonatal 9.4
1328 hemorrhage, intracerebral 9.4
1329 diarrhea 6 9.4
1330 periodic fever, menstrual cycle-dependent 9.4
1331 membranous nephropathy 9.4
1332 prostate cancer, hereditary, 2 9.4
1333 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.4
1334 leptin deficiency or dysfunction 9.4
1335 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 9.4
1336 pulmonary hypertension, primary, 3 9.4
1337 hyperprolactinemia 9.4
1338 pachyonychia congenita 3 9.4
1339 carbonic anhydrase va deficiency, hyperammonemia due to 9.4
1340 neu-laxova syndrome 2 9.4
1341 sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay 9.4
1342 cardiac conduction disease with or without dilated cardiomyopathy 9.4
1343 chops syndrome 9.4
1344 ring chromosome 14 syndrome 9.4
1345 lymphatic malformation 7 9.4
1346 mulchandani-bhoj-conlin syndrome 9.4
1347 actn3 deficiency 9.4
1348 alkuraya-kucinskas syndrome 9.4
1349 hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome 9.4
1350 neurodevelopmental disorder with cerebellar atrophy and with or without seizures 9.4
1351 fetal akinesia deformation sequence 2 9.4
1352 chronic ulcer of skin 9.4
1353 chronic diarrhea due to guanylate cyclase 2c overactivity 9.4
1354 stargardt disease 9.4
1355 adrenal cortical carcinoma 9.4
1356 keshan disease 9.4
1357 hemophagocytic lymphohistiocytosis 9.4
1358 tick-borne encephalitis 9.4
1359 erythema multiforme 9.4
1360 congenital hypothyroidism 9.4
1361 arrhythmogenic right ventricular cardiomyopathy 9.4
1362 usher syndrome 9.4
1363 visceral heterotaxy 9.4
1364 distal arthrogryposis 9.4
1365 alcohol-related birth defect 9.4
1366 chorioamnionitis 9.4
1367 vitamin b12 deficiency 9.4
1368 zollinger-ellison syndrome 9.4
1369 cone dystrophy 9.4
1370 tricuspid valve disease 9.4
1371 hemorrhagic cystitis 9.4
1372 tongue squamous cell carcinoma 9.4
1373 large cell neuroendocrine carcinoma 9.4
1374 colon adenoma 9.4
1375 writing disorder 9.4
1376 progesterone-receptor positive breast cancer 9.4
1377 brain glioma 9.4
1378 alexithymia 9.4
1379 microscopic colitis 9.4
1380 lymphocytic colitis 9.4
1381 ptosis 9.4
1382 umbilical hernia 9.4
1383 drug allergy 9.4
1384 spinal disease 9.4
1385 dextro-looped transposition of the great arteries 9.4
1386 physical disorder 9.4
1387 acromesomelic dysplasia 9.4
1388 myoglobinuria 9.4
1389 lymphoblastic lymphoma 9.4
1390 hepatic veno-occlusive disease 9.4
1391 chronic myelomonocytic leukemia 9.4
1392 superior semicircular canal dehiscence 9.4
1393 cakut 9.4
1394 alzheimer's disease 1 9.4
1395 endometrial hyperplasia 9.4
1396 lung non-squamous non-small cell carcinoma 9.4
1397 thyroid gland anaplastic carcinoma 9.4
1398 kleefstra syndrome 9.4
1399 benign teratoma 9.4
1400 sitosterolemia 9.4
1401 migraine with aura 9.4
1402 pelvic inflammatory disease 9.4
1403 asymptomatic neurosyphilis 9.4
1404 endometrial disease 9.4
1405 sleeping sickness 9.4
1406 trypanosomiasis 9.4
1407 cerebral artery occlusion 9.4
1408 venous insufficiency 9.4
1409 xerophthalmia 9.4
1410 cholelithiasis 9.4
1411 monocular esotropia 9.4
1412 asbestosis 9.4
1413 dentin caries 9.4
1414 osteomalacia 9.4
1415 mild pre-eclampsia 9.4
1416 lactose intolerance 9.4
1417 interstitial nephritis 9.4
1418 juvenile glaucoma 9.4
1419 mastitis 9.4
1420 filariasis 9.4
1421 gastric ulcer 9.4
1422 hand, foot and mouth disease 9.4
1423 lepromatous leprosy 9.4
1424 hypospadias 9.4
1425 microcephaly 9.4
1426 borderline personality disorder 9.4
1427 meconium aspiration syndrome 9.4
1428 placenta praevia 9.4
1429 leech infestation 9.4
1430 esophageal varix 9.4
1431 allergic conjunctivitis 9.4
1432 orbital cellulitis 9.4
1433 anemia of prematurity 9.4
1434 gingival recession 9.4
1435 epidural abscess 9.4
1436 alternating exotropia 9.4
1437 exotropia 9.4
1438 cardiac tamponade 9.4
1439 suppurative otitis media 9.4
1440 hypertensive heart disease 9.4
1441 hypertensive retinopathy 9.4
1442 hyperandrogenism 9.4
1443 choledocholithiasis 9.4
1444 hepatorenal syndrome 9.4
1445 coronary thrombosis 9.4
1446 tibial neuropathy 9.4
1447 gastroparesis 9.4
1448 hemosiderosis 9.4
1449 pica disease 9.4
1450 tympanosclerosis 9.4
1451 filarial elephantiasis 9.4
1452 anisometropia 9.4
1453 varicocele 9.4
1454 retroperitoneal sarcoma 9.4
1455 shigellosis 9.4
1456 vulva cancer 9.4
1457 pancytopenia 9.4
1458 secondary hyperparathyroidism 9.4
1459 hemolytic-uremic syndrome 9.4
1460 dyscalculia 9.4
1461 nephrocalcinosis 9.4
1462 acoustic neuroma 9.4
1463 hereditary hemorrhagic telangiectasia 9.4
1464 cerebral atherosclerosis 9.4
1465 migraine without aura 9.4
1466 keratoconjunctivitis sicca 9.4
1467 shipyard eye 9.4
1468 balanitis 9.4
1469 renal osteodystrophy 9.4
1470 paronychia 9.4
1471 right bundle branch block 9.4
1472 klebsiella pneumonia 9.4
1473 reading disorder 9.4
1474 urethritis 9.4
1475 coccidioidomycosis 9.4
1476 scleritis 9.4
1477 tuberous sclerosis 9.4
1478 kwashiorkor 9.4
1479 biliary atresia 9.4
1480 campylobacteriosis 9.4
1481 beriberi 9.4
1482 hepatic infarction 9.4
1483 opisthorchiasis 9.4
1484 pharyngoconjunctival fever 9.4
1485 amenorrhea 9.4
1486 bipolar i disorder 9.4
1487 tracheal calcification 9.4
1488 chronic purulent otitis media 9.4
1489 adult-onset still's disease 9.4
1490 pulmonary valve insufficiency 9.4
1491 dumping syndrome 9.4
1492 olivopontocerebellar atrophy 9.4
1493 leber congenital amaurosis 9.4
1494 personality disorder 9.4
1495 panniculitis 9.4
1496 pleural disease 9.4
1497 dermatomycosis 9.4
1498 ectropion 9.4
1499 renovascular hypertension 9.4
1500 keratosis 9.4
1501 breast fibroadenoma 9.4
1502 benign breast phyllodes tumor 9.4
1503 skeletal tuberculosis 9.4
1504 ventricular septal defect 9.4
1505 neovascular glaucoma 9.4
1506 endocrine gland cancer 9.4
1507 richter's syndrome 9.4
1508 vascular cancer 9.4
1509 mitral valve stenosis 9.4
1510 thyroid gland cancer 9.4
1511 pericarditis 9.4
1512 peritoneal mesothelioma 9.4
1513 cannabis dependence 9.4
1514 atrial heart septal defect 9.4
1515 leiomyosarcoma 9.4
1516 thymus lipoma 9.4
1517 hepatitis d 9.4
1518 heel spur 9.4
1519 enamel caries 9.4
1520 essential thrombocythemia 9.4
1521 myeloproliferative neoplasm 9.4
1522 vulvovaginitis 9.4
1523 hidradenitis suppurativa 9.4
1524 hidradenitis 9.4
1525 arteriosclerosis 9.4
1526 macrocytic anemia 9.4
1527 renal artery disease 9.4
1528 protein s deficiency 9.4
1529 retinal vascular disease 9.4
1530 motor peripheral neuropathy 9.4
1531 angiodysplasia 9.4
1532 tooth erosion 9.4
1533 orchitis 9.4
1534 chondromalacia 9.4
1535 ovarian brenner tumor 9.4
1536 cystic teratoma 9.4
1537 transitional cell carcinoma 9.4
1538 ossifying fibromyxoid tumor 9.4
1539 myoma 9.4
1540 acrodermatitis 9.4
1541 cerebellar disease 9.4
1542 hemoglobin c disease 9.4
1543 hemoglobinopathy 9.4
1544 glucosephosphate dehydrogenase deficiency 9.4
1545 aleutian mink disease 9.4
1546 cockayne syndrome 9.4
1547 bursitis 9.4
1548 carbohydrate metabolic disorder 9.4
1549 antiphospholipid syndrome 9.4
1550 acinar cell carcinoma 9.4
1551 astrocytoma 9.4
1552 grade iii astrocytoma 9.4
1553 early myoclonic encephalopathy 9.4
1554 cystic lymphangioma 9.4
1555 gingival overgrowth 9.4
1556 papillary carcinoma 9.4
1557 gallbladder cancer 9.4
1558 neurilemmoma 9.4
1559 syringomyelia 9.4
1560 embryonal carcinoma 9.4
1561 neurodermatitis 9.4
1562 gm2 gangliosidosis 9.4
1563 localized osteosarcoma 9.4
1564 bacterial vaginosis 9.4
1565 breast disease 9.4
1566 mastocytosis 9.4
1567 gallbladder adenocarcinoma 9.4
1568 lung benign neoplasm 9.4
1569 plexopathy 9.4
1570 plasmacytoma 9.4
1571 protein c deficiency 9.4
1572 leukorrhea 9.4
1573 arthropathy 9.4
1574 thrombophlebitis 9.4
1575 placental insufficiency 9.4
1576 insulinoma 9.4
1577 adrenal cortical adenocarcinoma 9.4
1578 merkel cell carcinoma 9.4
1579 angioma serpiginosum 9.4
1580 malignant ovarian brenner tumor 9.4
1581 pyoderma 9.4
1582 coronary restenosis 9.4
1583 gait apraxia 9.4
1584 milk allergy 9.4
1585 large cell carcinoma 9.4
1586 intraocular retinoblastoma 9.4
1587 prostate disease 9.4
1588 atrophic rhinitis 9.4
1589 placenta accreta 9.4
1590 adenocarcinoma in situ 9.4
1591 gastroesophageal junction adenocarcinoma 9.4
1592 mixed glioma 9.4
1593 ovarian cyst 9.4
1594 hemangioblastoma 9.4
1595 blepharospasm 9.4
1596 pulmonary coin lesion 9.4
1597 lung adenoma 9.4
1598 lice infestation 9.4
1599 testicular germ cell cancer 9.4
1600 mature teratoma 9.4
1601 malignant syringoma 9.4
1602 gastrinoma 9.4
1603 acute pyelonephritis 9.4
1604 large intestine cancer 9.4
1605 retinal disease 9.4
1606 well-differentiated liposarcoma 9.4
1607 pleomorphic liposarcoma 9.4
1608 cerebral lymphoma 9.4
1609 inferior myocardial infarction 9.4
1610 mitral valve disease 9.4
1611 overnutrition 9.4
1612 diffuse idiopathic skeletal hyperostosis 9.4
1613 hepatoblastoma 9.4
1614 pseudosarcomatous fibromatosis 9.4
1615 carotid artery occlusion 9.4
1616 mediastinitis 9.4
1617 scabies 9.4
1618 afferent loop syndrome 9.4
1619 brachial plexus lesion 9.4
1620 pellagra 9.4
1621 actinomycosis 9.4
1622 polyhydramnios 9.4
1623 night blindness 9.4
1624 chronic fatigue syndrome 9.4
1625 pyoderma gangrenosum 9.4
1626 oral cavity cancer 9.4
1627 decubitus ulcer 9.4
1628 metagonimiasis 9.4
1629 rosacea 9.4
1630 chorioretinitis 9.4
1631 sideroblastic anemia 9.4
1632 cutaneous leishmaniasis 9.4
1633 dyskinesia of esophagus 9.4
1634 scotoma 9.4
1635 carotid artery dissection 9.4
1636 cannabis abuse 9.4
1637 smoldering myeloma 9.4
1638 bronchiectasis 9.4
1639 dextrocardia 9.4
1640 plantar fasciitis 9.4
1641 necrotizing fasciitis 9.4
1642 babesiosis 9.4
1643 tenosynovitis 9.4
1644 biliary tract disease 9.4
1645 diabetic neuropathy 9.4
1646 hemorrhoid 9.4
1647 xanthogranulomatous cholecystitis 9.4
1648 diastolic heart failure 9.4
1649 irritable bowel syndrome 9.4
1650 polyarteritis nodosa 9.4
1651 neonatal abstinence syndrome 9.4
1652 refractive error 9.4
1653 esotropia 9.4
1654 congenital syphilis 9.4
1655 hydrocele 9.4
1656 developmental coordination disorder 9.4
1657 hypoplastic left heart syndrome 9.4
1658 periostitis 9.4
1659 heterotaxy 9.4
1660 keloid disorder 9.4
1661 bcl11a-related intellectual disability 9.4
1662 dysferlinopathy 9.4
1663 dystrophinopathies 9.4
1664 isolated gonadotropin-releasing hormone deficiency 9.4
1665 prothrombin-related thrombophilia 9.4
1666 suclg1-related mitochondrial dna depletion syndrome, encephalomyopathic form with methylmalonic aciduria 9.4
1667 trichorhinophalangeal syndrome 9.4
1668 12q14 microdeletion syndrome 9.4
1669 allergic angiitis 9.4
1670 amaurosis fugax 9.4
1671 anaplastic oligodendroglioma 9.4
1672 aneurysm of sinus of valsalva 9.4
1673 aortic arch interruption 9.4
1674 auditory neuropathy spectrum disorder 9.4
1675 bk-virus nephropathy 9.4
1676 candida glabrata 9.4
1677 carcinoma showing thymus-like differentiation 9.4
1678 central serous chorioretinopathy 9.4
1679 cerebrospinal fluid leak 9.4
1680 cerulean cataract 9.4
1681 congenital contractures 9.4
1682 congenital torticollis 9.4
1683 cor triatriatum 9.4
1684 crystal arthropathies 9.4
1685 diencephalic syndrome 9.4
1686 diphallia 9.4
1687 disseminated infection with mycobacterium avium complex 9.4
1688 distomatosis 9.4
1689 double discordia 9.4
1690 doxorubicin induced cardiomyopathy 9.4
1691 encephalocele 9.4
1692 enteropathica 9.4
1693 exfoliative dermatitis 9.4
1694 familial colorectal cancer 9.4
1695 familial hypertension 9.4
1696 fetal and neonatal alloimmune thrombocytopenia 9.4
1697 fetal macrosomia 9.4
1698 fibromatosis 9.4
1699 gangliosidosis 9.4
1700 germ cells tumors 9.4
1701 growth hormone deficiency 9.4
1702 heavy metal poisoning 9.4
1703 heparin-induced thrombocytopenia 9.4
1704 homologous wasting disease 9.4
1705 hyperacusis 9.4
1706 logopenic progressive aphasia 9.4
1707 multifocal motor neuropathy 9.4
1708 mycobacterium fortuitum 9.4
1709 mycobacterium marinum 9.4
1710 neisseria meningitidis infection 9.4
1711 neonatal meningitis 9.4
1712 neurosyphilis 9.4
1713 pediatric ulcerative colitis 9.4
1714 periodontal ehlers-danlos syndrome 9.4
1715 postorgasmic illness syndrome 9.4
1716 precocious puberty 9.4
1717 primary orthostatic hypotension 9.4
1718 primary orthostatic tremor 9.4
1719 prosthetic joint infection 9.4
1720 pulmonary artery agenesis 9.4
1721 pyogenic granuloma 9.4
1722 reversible cerebral vasoconstriction syndrome 9.4
1723 single ventricular heart 9.4
1724 sirenomelia 9.4
1725 spondylarthropathy 9.4
1726 st anthony's fire 9.4
1727 systemic onset juvenile idiopathic arthritis 9.4
1728 tuberculous meningitis 9.4
1729 wallerian degeneration 9.4
1730 stargardt macular degeneration 9.4
1731 trnt1 deficiency 9.4
1732 abdominal wall defect 9.4
1733 age-related hearing loss 9.4
1734 congenital plasminogen deficiency 9.4
1735 core binding factor acute myeloid leukemia 9.4
1736 opioid addiction 9.4
1737 autonomic dysfunction 9.4
1738 cerebral aneurysms 9.4
1739 developmental dyspraxia 9.4
1740 febrile seizures 9.4
1741 persistent vegetative state 9.4
1742 pituitary tumors 9.4
1743 malignant peritoneal mesothelioma 9.4
1744 refractory anemia with excess blasts in transformation 9.4
1745 b-cell non-hodgkin lymphoma 9.4
1746 cleft lip/palate 9.4
1747 asbestos intoxication 9.4
1748 inflammatory myopathy with abundant macrophages 9.4
1749 angiocentric glioma 9.4
1750 uniparental disomy of chromosome 7 9.4
1751 isolated focal cortical dysplasia type ib 9.4
1752 isolated focal cortical dysplasia type ia 9.4
1753 isolated focal cortical dysplasia type i 9.4
1754 qualitative or quantitative defects of dystrophin 9.4
1755 qualitative or quantitative defects of dysferlin 9.4
1756 rare hereditary hemochromatosis 9.4
1757 acute pandysautonomia 9.4
1758 ring chromosome 9.4
1759 lmna-related cardiocutaneous progeria syndrome 9.4
1760 rare odontogenic tumor 9.4
1761 acyl-coa dehydrogenase deficiency 9.4
1762 avascular necrosis 9.4
1763 malignant epithelial tumor of ovary 9.4
1764 lethal neonatal spasticity-epileptic encephalopathy syndrome 9.4
1765 secondary sclerosing cholangitis 9.4
1766 erythema multiforme major 9.4
1767 ethylene glycol poisoning 9.4
1768 congenital amyoplasia 9.4
1769 argyria 9.4
1770 parenteral nutrition-associated cholestasis 9.4
1771 rasopathy 9.4
1772 anterior cutaneous nerve entrapment syndrome 9.4
1773 serotonin syndrome 9.4
1774 acute liver failure 9.4
1775 lymphedema 9.4
1776 premature aging 9.4
1777 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 9.4
1778 maternal uniparental disomy 9.4
1779 cleft mitral valve 9.4
1780 thrombotic microangiopathy 9.4
1781 right aortic arch 9.4
1782 refractory anemia 9.4
1783 congenital alacrima 9.4
1784 vitreoretinopathy 9.4
1785 precursor t-cell acute lymphoblastic leukemia 9.4
1786 autoimmune disease of peripheral nervous system 9.4 MPZ MOG MBP DPYSL5 CD40LG AQP4
1787 autoimmune disease of central nervous system 9.3 MOG MBP IL1B IL10 HLA-DRB1 CD40LG
1788 cranial nerve disease 9.3 MOG MBP DPYSL5 CD40LG CCR6 AQP4
1789 thymus gland disease 9.2 LGI1 DPYSL5 CNTNAP2 CD40LG CCR6
1790 thymus cancer 9.2 LGI1 DPYSL5 CNTNAP2 CD40LG CCR6
1791 lymphatic system cancer 9.0 LGI1 DPYSL5 CSF3 CNTNAP2 CD40LG CCR6
1792 spinal cord disease 8.8 MOG MBP LGI1 IL10 DPYSL5 CD40LG
1793 neuromuscular junction disease 8.8 LGI1 IL10 DPYSL5 CNTNAP2 CD40LG CCR6
1794 neuromuscular disease 8.4 MPZ MBP LGI1 IL10 DPYSL5 CNTNAP2

Graphical network of the top 20 diseases related to Acute Disseminated Encephalomyelitis:



Diseases related to Acute Disseminated Encephalomyelitis

Symptoms & Phenotypes for Acute Disseminated Encephalomyelitis

MGI Mouse Phenotypes related to Acute Disseminated Encephalomyelitis:

45 (showing 3, show less)
# Description MGI Source Accession Score Top Affiliating Genes
1 hematopoietic system MP:0005397 9.93 AQP4 CCR6 CD40LG CDH23 CSF3 HLA-DQA1
2 immune system MP:0005387 9.73 AQP4 CCR6 CD40LG CDH23 CSF3 HLA-DQA1
3 nervous system MP:0003631 9.47 AQP4 CCR6 CD40LG CDH23 CNTNAP2 DPYSL5

Drugs & Therapeutics for Acute Disseminated Encephalomyelitis

Drugs for Acute Disseminated Encephalomyelitis (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(showing 26, show less)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1 Vaccines Phase 4
2 Antibodies, Blocking Phase 4
3
Methylprednisolone hemisuccinate Approved Phase 3 2921-57-5
4
Methylprednisolone Approved, Vet_approved Phase 3 83-43-2 6741
5
Prednisolone Approved, Vet_approved Phase 3 50-24-8 5755
6 Prednisolone acetate Approved, Vet_approved Phase 3 52-21-1
7
Prednisolone phosphate Approved, Vet_approved Phase 3 302-25-0
8
Prednisolone hemisuccinate Experimental Phase 3 2920-86-7
9 Methylprednisolone Acetate Phase 3
10
rituximab Approved Phase 2 174722-31-7 10201696
11 Antibodies Phase 2
12 Immunoglobulins Phase 2
13 Immunologic Factors Phase 2
14 Antineoplastic Agents, Immunological Phase 2
15 Antirheumatic Agents Phase 2
16 Autoantibodies
17 Anti-Bacterial Agents
18 interferons
19 Anti-Infective Agents
20 Antibiotics, Antitubercular
21 Adjuvants, Immunologic
22 Antiviral Agents
23 Protective Agents
24 polysaccharide-K
25 Radiation-Protective Agents
26 Interferon Inducers

Interventional clinical trials:

(showing 12, show less)
# Name Status NCT ID Phase Drugs
1 Neutralizing Antibody Titers 6 Years After the Third Dose of Inactivated Japanese Encephalitis Vaccine and Projected Duration of Protection Completed NCT02039440 Phase 4
2 Phase III Randomized, Double-Blind, Sham-Controlled Study of Plasma Exchange for Acute Severe Attacks of Inflammatory Demyelinating Disease Refractory to Intravenous Methylprednisolone Unknown status NCT00004645 Phase 3
3 Randomized Clinical Trial of Plasma Exchanges Versus Sham Plasma Exchanges in Disabling Multiple Sclerosis Acute Relapses Refractory to Steroid Treatment Completed NCT01442233 Phase 3
4 Prospective Assessment of Efficacy of Immunoadsorption Therapy in Managing Childhood NMDA-Receptor (NMDAR) Antibodies Encephalitis Not yet recruiting NCT03274375 Phase 2 IA session;Rituximab
5 Management of Acute Disseminated Encephalomyelitis in Neurology Unit of Assiut University Children Hospital Unknown status NCT03284801
6 Observational Prospective Multicentered Study Evaluating Initial Clinical Presentation of Inflammatory Optic Neuritis (ON) Associated or Not With Autoantibodies Anti- Myelin-oligodendrocyte-glycoprotein (MOG-Ab) Unknown status NCT03345537
7 Pediatric Multiple Sclerosis in Egypt. A Multi-center Registry of 186 Patients Completed NCT03360188
8 A Phase IV Study to Assess the Safety of Menveo Vaccine Being Used by HMO Subjects Aged 11-21 Years of Age Completed NCT01452464
9 PEDIATRIC SONICS: Pediatric Study of Neuropsychology and Imaging in CNS Demyelinating Syndromes. Recruiting NCT03942952
10 A Multicenter Observational Study to Evaluate Pediatric Multiple Sclerosis in Brazil Recruiting NCT03087136
11 Epidemiology and Prognosis of Encephalitis in Intensive Care Recruiting NCT02906631
12 Large-scale, Multi-disciplinary Sample and Data Repository for Multiple Sclerosis and Related Demyelinating Diseases Active, not recruiting NCT00445367

Search NIH Clinical Center for Acute Disseminated Encephalomyelitis

Genetic Tests for Acute Disseminated Encephalomyelitis

Anatomical Context for Acute Disseminated Encephalomyelitis

MalaCards organs/tissues related to Acute Disseminated Encephalomyelitis:

40
Brain, Spinal Cord, Heart, Thyroid, Lung, Bone, Eye

Publications for Acute Disseminated Encephalomyelitis

Articles related to Acute Disseminated Encephalomyelitis:

(showing 1621, show less)
# Title Authors PMID Year
1
Doxycycline in autoimmune central nervous system disorders in children: an in vitro study. 54 61
17990580 2007
2
Hypersomnia and low cerebrospinal fluid hypocretin levels in acute disseminated encephalomyelitis. 54 61
15519122 2004
3
Structural similarity between the bee venom peptides and the immunodominant human myelin basic proteins: role for pathogenesis of acute disseminated encephalomyelitis. 54 61
12589368 2003
4
A case of acute disseminated encephalomyelitis presenting hypersomnia with decreased hypocretin level in cerebrospinal fluid. 54 61
12269735 2002
5
Heat shock protein immunoreactivity in CSF: correlation with oligoclonal banding and demyelinating disease. 54 61
7936289 1994
6
Overlapping autoimmune syndrome: A case of concomitant anti-NMDAR encephalitis and myelin oligodendrocyte glycoprotein (MOG) antibody disease. 61
31837635 2020
7
Variation in Treatment and Outcomes of Children With Acute Disseminated Encephalomyelitis. 61
31996356 2020
8
Acute Disseminated Encephalomyelitis followed by Optic Neuritis: A Rare Syndrome of Uncertain Treatment and Prognosis. 61
31935763 2020
9
Extensive subpial cortical demyelination is specific to multiple sclerosis. 61
31916298 2020
10
Acute disseminated encephalomyelitis (ADEM) associated with mosquito-borne diseases: Chikungunya virus X yellow fever immunization. 61