Multiple Sclerosis, Susceptibility To; Ms
Genes related to Multiple Sclerosis, Susceptibility To; Ms
- HLA-DQB1
- HLA-DRB1
- PDCD1
Clinical Features
Top most frequent phenotypes and symptoms related to Multiple Sclerosis, Susceptibility To; Ms
- Seizures
- Hearing impairment
- Nystagmus
- Neoplasm
- Muscle weakness
- Pain
- Spasticity
- Visual impairment
- Hyperreflexia
- Tremor
And another 19 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Multiple Sclerosis, Susceptibility To; Ms Is also known as disseminated sclerosis.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Multiple Sclerosis, Susceptibility To; Ms Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 Narcolepsy (HLA-DQB1 06:02) Genotyping.
By ARUP Laboratories, Molecular Genetics and Genomics (United States).
HLA-DQB1
Specificity
100 %
Genes
34 % |
|
Celiac Disease (HLA-DQ2 and HLA-DQ8) Genotyping.
By ARUP Laboratories, Molecular Genetics and Genomics (United States).
HLA-DQA1, HLA-DQB1
Specificity
50 %
Genes
34 % |
 Celiac disease (HLA-DQ/DR).
By CGC Genetics (Portugal).
HLA-DQA1, HLA-DQB1
Specificity
50 %
Genes
34 % |
|
Lactose intolerance (MCM6 gene) and Celiac disease (HLA-DQ2/ HLA-DQ8).
By CGC Genetics (Portugal).
HLA-DQA1, HLA-DQB1, MCM6
Specificity
34 %
Genes
34 % |
|
Celiac Disease via Next Generation Sequencing HLA Typing.
By PreventionGenetics PreventionGenetics (United States).
HLA-DQA1, HLA-DQB1
Specificity
50 %
Genes
34 % |
 Narcolepsy Risk Factor.
By Bioscientia GmbH Center for Human Genetics (Germany).
HLA-DQB1, HLA-DRB1
Specificity
100 %
Genes
67 % |
 HLA DQ2/DQ8.
By Furst Medical Laboratories, FurstNAT (Norway).
HLA-DQA1, HLA-DQB1
Specificity
50 %
Genes
34 % |
 Celiac Disease (HLA-DQA1*05, HLA-DQB1*02, and HLA-DQB1*03:02) Genotyping.
By Molecular Genetics Laboratory Centro de Investigaciones Endocrinologicas "Dr. Cesar Bergada" (Argentina).
HLA-DQA1, HLA-DQB1
Specificity
50 %
Genes
34 % |
You can get up to 8 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SPINOCEREBELLAR ATAXIA 28; SCA28 MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION; FESD FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1; FCAS1 ICHTHYOSIS VULGARIS CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M