/inherited susceptibility to mycobacterial diseases

/autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency

autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency

Rare Disease

MONDO:0014710

Also Known As

IMD42RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiencyautosomal recessive MSMD due to complete RORgamma receptor defiencyautosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in RORCautosomal recessive primary immunodeficiency due to RORC mutationimmunodeficiency 42immunodeficiency type 42

Definition

Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the RORC gene.

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Associated Genes

RORC ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616622 ↗

Orphanet

Orphanet:477857 ↗

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