All diseases

OMIM ID
228900
OMIM term:
FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY
Alternative terms:

(∗) Location:
20q11.22  
(†) Associated OMIM genes:
GDF5  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/6uwmqg4z