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Herpetic encephalitis
4 OMIM references -
5 associated genes
124 connected diseases
No signs/symptoms info
Disease Type of connection
Common variable immunodeficiency
Autosomal dominant hypohidrotic ectodermal dysplasia
Hypohidrotic ectodermal dysplasia with immunodeficiency
Behçet disease
Cerebellar ataxia - hypogonadism
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Amyotrophic lateral sclerosis
Chronic mucocutaneous candidiasis
Translocation renal cell carcinoma
Pyogenic bacterial infections due to MyD88 deficiency
Waldenström macroglobulinemia
Giant cell glioblastoma
Gliosarcoma
Papillary or follicular thyroid carcinoma
Extraskeletal myxoid chondrosarcoma
Cardiofaciocutaneous syndrome
Autosomal dominant nonsyndromic intellectual deficit
Familial expansile osteolysis
Osteopetrosis - hypogammaglobulinemia
Hyper-IgM syndrome type 3
X-linked hypohidrotic ectodermal dysplasia
Autosomal agammaglobulinemia
SHORT syndrome
Anaplastic ependymoma
MULIBREY nanism
MALT lymphoma
Autosomal recessive lymphoproliferative disease
X-linked lymphoproliferative disease
Familial infantile bilateral striatal necrosis
Solitary fibrous tumor
Familial cylindromatosis
Familial multiple trichoepithelioma
Autosomal recessive spastic ataxia - optic atrophy - dysarthria
Left ventricular noncompaction
Precursor T-cell acute lymphoblastic leukemia
Blackfan-Diamond anemia
Catecholaminergic polymorphic ventricular tachycardia
Fragile X syndrome
Fragile X-associated tremor / ataxia syndrome
Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency
Hereditary sensory and autonomic neuropathy with spastic paraplegia
Hypomyelination with atrophy of basal ganglia and cerebellum
Isolated ATP synthase deficiency
Primary dystonia, DYT4 type
Split hand-split foot malformation
Wolf-Hirschhorn syndrome
Xq27.3q28 duplication syndrome
Pediatric systemic lupus erythematosus
Adult hypophosphatasia
Autosomal recessive hypohidrotic ectodermal dysplasia
Childhood-onset hypophosphatasia
Diffuse cutaneous systemic sclerosis
Infantile hypophosphatasia
Limited cutaneous systemic sclerosis
Odontohypophosphatasia
Perinatal lethal hypophosphatasia
Prenatal benign hypophosphatasia
Primary biliary cirrhosis
17p13.3 microduplication syndrome
Adult Krabbe disease
CEDNIK syndrome
Cerebro-facio-thoracic dysplasia
Chronic myelomonocytic leukemia
Congenital mesoblastic nephroma
Craniopharyngioma
DDOST-CDG
Desmoplastic small round cell tumor
Developmental delay with autism spectrum disorder and gait instability
Distal 17p13.3 microdeletion syndrome
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
Ewing sarcoma
Extraskeletal Ewing sarcoma
Familial hemophagocytic lymphohistiocytosis
Fibrosarcoma
Hairy cell leukemia
Hashimoto-Pritzker syndrome
Hereditary motor and sensory neuropathy, Okinawa type
Hereditary thrombophilia due to congenital protein S deficiency
Infantile Krabbe disease
LEOPARD syndrome
Late-infantile / juvenile Krabbe disease
Melanoma of soft part
Miller-Dieker syndrome
Multiple congenital anomalies - hypotonia - seizures syndrome
Niemann-Pick disease type C, adult neurologic onset
Niemann-Pick disease type C, juvenile neurologic onset
Niemann-Pick disease type C, late infantile neurologic onset
Niemann-Pick disease type C, severe early infantile neurologic onset
Niemann-Pick disease type C, severe perinatal form
Noonan syndrome
Pilocytic astrocytoma
Precursor B-cell acute lymphoblastic leukemia
Renal tubular dysgenesis of genetic origin
STT3A-CDG
STT3B-CDG
Spastic paraplegia-optic atrophy-neuropathy syndrome
Young adult-onset Parkinsonism
Autoimmune lymphoproliferative syndrome
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Intermittent hydrarthrosis
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
TRAPS syndrome
CLOVE syndrome
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Cowden syndrome
Hemimegalencephaly
Hereditary nonpolyposis colon cancer
Intermediate nemaline myopathy
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Severe congenital nemaline myopathy
Typical nemaline myopathy
Synonym(s):
- HSV encephalitis
- Herpes simplex encephalitis
- Herpes simplex neuroinvasion
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare infectious disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: any age
Type of inheritance: sporadic
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.