(Q28065574)

English

T-cell immunodeficiency, congenital alopecia, and nail dystrophy

severe combined immunodeficiency characterized by congenital alopecia, severe T-cell immunodeficiency, and ridging, pitting or curving of all nails that has material basis in homozygous mutation in the FOXN1 gene on chromosome 17q11-q12

  • alymphoid cystic thymic dysgenesis
  • severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome
  • winged helix deficiency
  • FOXN1 deficiency
  • alopecia immunodeficiency
  • T-cell immunodeficiency, congenital alopecia and nail dystrophy
  • T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY
  • Pignata Guarino syndrome
  • Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency

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