All diseases

OMIM ID
601705
OMIM term:
T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY
Alternative terms:

(∗) Location:
17q11.2  
(†) Associated OMIM genes:
FOXN1  
(‡) Associated MGI genes:
Foxn1  

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* quick link - http://q.sanger.ac.uk/a5sse86g