All diseases

OMIM ID
186000
OMIM term:
SYNPOLYDACTYLY 1; SPD1
Alternative terms:

(∗) Location:
2q31.1  
(†) Associated OMIM genes:
HOXD13  
(‡) Associated MGI genes:
Hoxd13  

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* quick link - http://q.sanger.ac.uk/a3hnpy6h