All diseases

OMIM ID
166250
OMIM term:
OSTEOGLOPHONIC DYSPLASIA; OGD
Alternative terms:

(∗) Location:
8p11.23-p11.22  
(†) Associated OMIM genes:
FGFR1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jrkgahh6