All diseases

OMIM ID
178300
OMIM term:
PTOSIS, HEREDITARY CONGENITAL 1; PTOS1
Alternative terms:

(∗) Location:
1p34.1-p32   8q21.11  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/zusf53h1