All diseases

OMIM ID
609428
OMIM term:
TUKEL SYNDROME
Alternative terms:
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH ULNAR HAND ANOMALIES
CFEOM-U
(∗) Location:
21q22  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/807ut6kf