T-cell immunodeficiency, congenital alopecia, and nail dystrophy (Q28065574)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
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