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Immunodeficiency 76
rareAn autosomal recessive primary immunologic disorder characterized by onset of recurrent bacterial, viral, and fungal infections in early childhood. Laboratory studies show T-cell lymphopenia and may show variable B-cell or immunoglobulin abnormalities. More variable features found in some patients include lymphoma and neurologic features. Although bone marrow transplantation may be curative, many patients die in childhood.
- Identifiers
- MONDO:0030898 OMIM:619164Orphanet:647804
- Causal genes
- FCHO1
- Part of
- Immunodeficiency disease
- Also known as
- combined immunodeficiency due to FCHO1 deficiency · IMD76 · immunodeficiency due to FCHO1 deficiency
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