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encyclopedia of Rare Disease Annotation for Precision Medicine

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	reye syndrome

Disease ID	975
Disease	reye syndrome
Definition	A form of encephalopathy with fatty infiltration of the LIVER, characterized by brain EDEMA and VOMITING that may rapidly progress to SEIZURES; COMA; and DEATH. It is caused by a generalized loss of mitochondrial function leading to disturbances in fatty acid and CARNITINE metabolism.
Synonym	fatty liver with encephalopathy reye 's syndrome reye johnson syndrome reye syndrome [disease/finding] reye's encephalopathy reye's syndrome reye's syndrome (disorder) reye-johnson syndrome reyes syndrome reyes syndromes reyes's syndrome syndrome reye syndrome reyes
Orphanet	ORPHANET:3096
DOID	DOID:14525
ICD10	ICD10CM:G93.7
UMLS	C0035400
MeSH	D012202
SNOMED-CT	SNOMEDCT_US_2016_09_01:74351001
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:3) C0042769 \| virus infection \| 1 C0014070 \| encephalomyelitis \| 1 C0021400 \| influenza \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:42) 2 \| A2M \| 1.032 \| DISEASES 31 \| ACACA \| 1.638 \| DISEASES 34 \| ACADM \| 2.341 \| DISEASES 229 \| ALDOB \| 3.228 \| DISEASES 279 \| AMY2A \| 1.969 \| DISEASES 840 \| CASP7 \| 1.329 \| DISEASES 6364 \| CCL20 \| 1.061 \| DISEASES 959 \| CD40LG \| 1.989 \| DISEASES 3426 \| CFI \| 1.808 \| DISEASES 1376 \| CPT2 \| 1.918 \| DISEASES 1431 \| CS \| 1.914 \| DISEASES 1555 \| CYP2B6 \| 1.985 \| DISEASES 1576 \| CYP3A4 \| 1.551 \| DISEASES 1612 \| DAPK1 \| 1.338 \| DISEASES 1743 \| DLST \| 3.243 \| DISEASES 3266 \| ERAS \| 1.034 \| DISEASES 2110 \| ETFDH \| 3.528 \| DISEASES 1647 \| GADD45A \| 1.364 \| DISEASES 2805 \| GOT1 \| 2.533 \| DISEASES 3033 \| HADH \| 1.823 \| DISEASES 3030 \| HADHA \| 4.485 \| DISEASES 3155 \| HMGCL \| 4.159 \| DISEASES 3376 \| IARS \| 1.287 \| DISEASES 3988 \| LIPA \| 1.732 \| DISEASES 987 \| LRBA \| 1.682 \| DISEASES 4049 \| LTA \| 1.009 \| DISEASES 4155 \| MBP \| 1.222 \| DISEASES 9968 \| MED12 \| 1.794 \| DISEASES 4508 \| MT-ATP6 \| 1.703 \| DISEASES 4512 \| MT-CO1 \| 1.396 \| DISEASES 4513 \| MT-CO2 \| 1.825 \| DISEASES 4514 \| MT-CO3 \| 2.664 \| DISEASES 4519 \| MT-CYB \| 1.339 \| DISEASES 4558 \| MT-TF \| 2.99 \| DISEASES 4566 \| MT-TK \| 1.25 \| DISEASES 6256 \| RXRA \| 1.777 \| DISEASES 23410 \| SIRT3 \| 1.305 \| DISEASES 6649 \| SOD3 \| 1.801 \| DISEASES 706 \| TSPO \| 1.23 \| DISEASES 7295 \| TXN \| 2.112 \| DISEASES 10628 \| TXNIP \| 2.628 \| DISEASES 23038 \| WDTC1 \| 2.957 \| DISEASES
Locus	(Waiting for update.)

Disease ID	975
Disease	reye syndrome
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:2) HP:0001298 \| Encephalopathy \| 1 HP:0001399 \| Liver failure \| 1

Disease ID	975
Disease	reye syndrome
Manually Symptom	UMLS \| Name(Total Manually Symptoms:9) C2364324 \| increased intracranial pressure C1963198 \| pancreatitis C1963101 \| encephalopathy C0151740 \| elevated intracranial pressure C0042769 \| viral infections C0037769 \| west syndrome C0022660 \| acute renal failure C0005779 \| coagulation defect C0002063 \| alkalosis
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0085584 \| encephalopathy \| 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	975
Disease	reye syndrome
Case	(Waiting for update.)

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