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encyclopedia of Rare Disease Annotation for Precision Medicine

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	myelitis

Disease ID	1574
Disease	myelitis
Definition	Inflammation of the spinal cord. Relatively common etiologies include infections; AUTOIMMUNE DISEASES; SPINAL CORD; and ischemia (see also SPINAL CORD VASCULAR DISEASES). Clinical features generally include weakness, sensory loss, localized pain, incontinence, and other signs of autonomic dysfunction.
Synonym	inflamm spinal cord inflammation of spinal cord inflammation, spinal cord inflammations, spinal cord inflammatory myelopathies inflammatory myelopathy myelitides myelitis (disorder) myelitis [disease/finding] myelitis, nos myelopathies, inflammatory myelopathy inflamm myelopathy, inflammatory spinal cord inflamm spinal cord inflammation spinal cord inflammations
DOID	DOID:322
UMLS	C0026975
MeSH	D009187
SNOMED-CT	SNOMEDCT_US_2016_09_01:41370002
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:51) C0024141 \| systemic lupus erythematosus \| 5 C0027873 \| neuromyelitis optica \| 4 C0004943 \| behcet's disease \| 4 C0019158 \| hepatitis \| 3 C0026769 \| multiple sclerosis \| 3 C0025289 \| meningitis \| 3 C0027813 \| neuritis \| 3 C0030486 \| paraplegia \| 3 C0409974 \| lupus erythematosus \| 3 C1527336 \| sjogren's syndrome \| 2 C0014038 \| encephalitis \| 2 C0019196 \| hepatitis c \| 2 C0029134 \| optic neuritis \| 2 C0021400 \| influenza \| 2 C0085273 \| parvovirus b19 infection \| 2 C0040558 \| toxoplasmosis \| 2 C0002895 \| sickle cell anemia \| 2 C1527336 \| sjogren syndrome \| 2 C0014059 \| acute disseminated encephalomyelitis \| 2 C0270629 \| epidural abscess \| 2 C0021053 \| immune disease \| 2 C0011603 \| dermatitis \| 1 C0206141 \| idiopathic hypereosinophilic syndrome \| 1 C0024530 \| malaria \| 1 C0009447 \| common variable immunodeficiency \| 1 C0011303 \| demyelinating disease \| 1 C0003872 \| psoriatic arthritis \| 1 C0019196 \| viral hepatitis c \| 1 C0021053 \| immune disorders \| 1 C0042769 \| virus infection \| 1 C0021053 \| immune disorder \| 1 C0154652 \| eosinophilic meningitis \| 1 C0042769 \| viral infection \| 1 C1145670 \| respiratory failure \| 1 C0235025 \| motor neuropathy \| 1 C0011303 \| demyelinating diseases \| 1 C0494491 \| mononeuropathy \| 1 C0085278 \| antiphospholipid syndrome \| 1 C0015230 \| rash \| 1 C0024537 \| vivax malaria \| 1 C0025309 \| meningoencephalitis \| 1 C0042170 \| harada disease \| 1 C0026848 \| myopathy \| 1 C0003708 \| arachnoiditis \| 1 C0085278 \| antiphospholipid antibody syndrome \| 1 C0042721 \| viral hepatitis \| 1 C0011615 \| atopic dermatitis \| 1 C0206141 \| hypereosinophilic syndrome \| 1 C0009241 \| cognitive disorders \| 1 C0042170 \| vogt-koyanagi-harada disease \| 1 C0032285 \| pneumonia \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:54) 199 \| AIF1 \| 1.105 \| DISEASES 273 \| AMPH \| 3.759 \| DISEASES 51378 \| ANGPT4 \| 2.031 \| DISEASES 361 \| AQP4 \| 7.868 \| DISEASES 9140 \| ATG12 \| 1.074 \| DISEASES 617 \| BCS1L \| 1.633 \| DISEASES 930 \| CD19 \| 1.695 \| DISEASES 23607 \| CD2AP \| 1.683 \| DISEASES 959 \| CD40LG \| 4.266 \| DISEASES 30850 \| CDR2L \| 2.588 \| DISEASES 1041 \| CDSN \| 1.892 \| DISEASES 1267 \| CNP \| 1.568 \| DISEASES 26047 \| CNTNAP2 \| 1.681 \| DISEASES 9244 \| CRLF1 \| 1.83 \| DISEASES 1471 \| CST3 \| 1.401 \| DISEASES 50624 \| CUZD1 \| 2.462 \| DISEASES 1630 \| DCC \| 1.282 \| DISEASES 51428 \| DDX41 \| 2.547 \| DISEASES 115352 \| FCRL3 \| 1.266 \| DISEASES 2235 \| FECH \| 2.418 \| DISEASES 2550 \| GABBR1 \| 1.56 \| DISEASES 2591 \| GALNT3 \| 2.471 \| DISEASES 2618 \| GART \| 1.268 \| DISEASES 54584 \| GNB1L \| 1.676 \| DISEASES 3115 \| HLA-DPB1 \| 2.527 \| DISEASES 3123 \| HLA-DRB1 \| 1.235 \| DISEASES 8091 \| HMGA2 \| 1.008 \| DISEASES 3456 \| IFNB1 \| 3.311 \| DISEASES 3605 \| IL17A \| 1.238 \| DISEASES 102723508 \| KANTR \| 2.076 \| DISEASES 84148 \| KAT8 \| 1.326 \| DISEASES 11202 \| KLK8 \| 1.141 \| DISEASES 137994 \| LETM2 \| 3.046 \| DISEASES 4155 \| MBP \| 3.651 \| DISEASES 50488 \| MINK1 \| 1.49 \| DISEASES 4340 \| MOG \| 5.415 \| DISEASES 246734 \| NPCDR1 \| 1.777 \| DISEASES 27445 \| PCLO \| 1.184 \| DISEASES 5133 \| PDCD1 \| 1.069 \| DISEASES 10687 \| PNMA2 \| 1.642 \| DISEASES 5542 \| PRB1 \| 1.871 \| DISEASES 23186 \| RCOR1 \| 1.713 \| DISEASES 5996 \| RGS1 \| 1.438 \| DISEASES 6229 \| RPS24 \| 1.545 \| DISEASES 123228 \| SENP8 \| 1.575 \| DISEASES 6656 \| SOX1 \| 1.261 \| DISEASES 55576 \| STAB2 \| 2.195 \| DISEASES 7124 \| TNF \| 1.23 \| DISEASES 7133 \| TNFRSF1B \| 2 \| DISEASES 10673 \| TNFSF13B \| 1.376 \| DISEASES 90249 \| UNC5A \| 1.891 \| DISEASES 7433 \| VIPR1 \| 1.033 \| DISEASES 340152 \| ZC3H12D \| 1.317 \| DISEASES 84107 \| ZIC4 \| 2.046 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1574
Disease	myelitis
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:30) HP:0010550 \| Paraplegia \| 4 HP:0002725 \| Systemic lupus erythematosus \| 4 HP:0003470 \| Inability to move \| 4 HP:0002960 \| Autoimmune condition \| 4 HP:0001287 \| Meningitis \| 3 HP:0012115 \| Liver inflammation \| 3 HP:0100653 \| Optic neuritis \| 2 HP:0002090 \| Pneumonia \| 2 HP:0100310 \| Extradural hematoma \| 2 HP:0003447 \| Axonal loss \| 2 HP:0100561 \| Spinal cord lesion \| 2 HP:0003613 \| Antiphospholipid antibodies \| 2 HP:0012531 \| Pain \| 2 HP:0002383 \| Encephalitis \| 2 HP:0000016 \| Urinary retention \| 2 HP:0002540 \| Inability to walk \| 1 HP:0000011 \| Neurogenic bladder \| 1 HP:0006532 \| Pneumonia, recurrent episodes \| 1 HP:0003198 \| Myopathic changes \| 1 HP:0001047 \| Atopic dermatitis \| 1 HP:0009733 \| Glioma \| 1 HP:0009831 \| Single damaged nerve \| 1 HP:0002385 \| Paraparesis \| 1 HP:0001880 \| Eosinophilia \| 1 HP:0000969 \| Dropsy \| 1 HP:0002414 \| Spina bifida \| 1 HP:0001907 \| Thromboembolic disease \| 1 HP:0000572 \| Visual loss \| 1 HP:0002878 \| Respiratory failure \| 1 HP:0006562 \| Viral hepatitis \| 1

Disease ID	1574
Disease	myelitis
Manually Symptom	UMLS \| Name(Total Manually Symptoms:5) C2127436 \| ascending paralysis C1000483 \| anemia C0031117 \| peripheral neuropathy C0014038 \| encephalitis C0007459 \| neurogenic bladder
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:2) C0014038 \| encephalitis \| 2 C0005697 \| neurogenic bladder \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	1574
Disease	myelitis
Case	(Waiting for update.)

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