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GTR Home > Conditions/Phenotypes > Mucocutaneous ulceration, chronic

Summary

Familial Behcet-like autoinflammatory disease-3 (AIFBL3) is an autosomal dominant disorder characterized predominantly by chronic mucocutaneous ulceration (summary by Lecerf et al., 2023). For a general phenotypic description and a discussion of genetic heterogeneity of AIFBL, see AIFBL1 (616744). [from OMIM]

Available tests

5 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: AIF3BL3, CMCU, NFKB3, p65, RELA
    Summary: RELA proto-oncogene, NF-kB subunit

Clinical features

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