| Human Phenotype
Ontology
|
Grandparent Node:
 Recurrent viral infections (HP:0004429) | Parent Node:
Recurrent herpes (HP:0005353) | ..Starting node
..Herpes simplex encephalitis (HP:0012302)
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| Term ID: |
12302 |
| Name: |
Herpes simplex encephalitis |
| Synonym: |
Herpes encephalitis |
| Definition: |
Infection of the brain parenchyma with herpes simplex virus, resulting in inflammation of the brain parenchyma with neurologic dysfunction. |
| Comments: |
|
| Reference: |
HP:0012302 |
| Genes and Diseases: | |
Child Nodes: |
Sister Nodes: | ..Kaposi's sarcoma (HP:0100726)
| ..Recurrent oral herpes (HP:0410028)
| | Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
|---|
HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | HYOU1 CL E G H | 10525 | 16931 | OMIM:233600 | Immunodeficiency 59 and hypoglycemia | | | | | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | NCKAP1L CL E G H | 3071 | 4862 | OMIM:618982 | IMMUNODEFICIENCY 72 WITH AUTOINFLAMMATION; IMD72 | | | | | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | SNORA31 CL E G H | 677814 | 32621 | OMIM:619396 | ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 10; IIAE10 | | | | | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | STAT1 CL E G H | 6772 | 11362 | OMIM:614892 | Immunodeficiency 31A | . | | | 89 | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | STAT1 CL E G H | 6772 | 11362 | OMIM:613796 | Mycobacterial and viral infections, susceptibility to, autosomal recessive | . | | | 89 | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | TBK1 CL E G H | 29110 | 11584 | OMIM:617900 | Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8 | . | | | 20 | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | TICAM1 CL E G H | 148022 | 18348 | OMIM:614850 | Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6 | . | | | 6 | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | TLR3 CL E G H | 7098 | 11849 | OMIM:613002 | Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 2 | . | | | 3 | | | | HP:0012302 | HP:0012302 | Herpes simplex encephalitis | 0 | UNC93B1 CL E G H | 81622 | 13481 | OMIM:610551 | ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 1; IIAE1 | | | | 5 | | |
Genes (8) :HYOU1 NCKAP1L SNORA31 STAT1 TBK1 TICAM1 TLR3 UNC93B1
Diseases (9) :OMIM:233600 OMIM:618982 OMIM:619396 OMIM:614892 OMIM:613796 OMIM:617900 OMIM:614850 OMIM:613002 OMIM:610551 |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
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