Agent Commons Collaborative Research
Immunodeficiency 80 with or without congenital cardiomyopathy
An autosomal recessive immunologic disorder with variable manifestations. One patient with infantile-onset of chronic cytomegalovirus (CMV) infection associated with severely decreased NK cells has been reported. Another family with 3 affected fetuses showing restrictive cardiomyopathy and hypoplasia of the spleen and thymus has also been reported.
- Identifiers
- MONDO:0030266 OMIM:619313
- Causal genes
- MCM10
- Part of
- Immunodeficiency disease
- Also known as
- IMD80 · immunodeficiency 80 with or without cardiomyopathy · immunodeficiency with or without congenital cardiomyopathy · MCM10 deficiency
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