autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency (Q55784947)
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human disease
- Autosomal recessive MSMD due to complete RORgamma receptor defiency
- Immunodeficiency type 42
- Immunodeficiency 42
- IMD42
- Autosomal recessive primary immunodeficiency due to RORC mutation
- immunodeficiency 42
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency |
human disease |
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