All diseases

OMIM ID
136760
OMIM term:
FRONTONASAL DYSPLASIA 1; FND1
Alternative terms:
FRONTORHINY
FRONTONASAL DYSPLASIA; FND
FRONTONASAL MALFORMATION; FNM
MEDIAN FACIAL CLEFT SYNDROME
(∗) Location:
1p13.3  
(†) Associated OMIM genes:
ALX3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/88b8aqio