All diseases

OMIM ID
176305
OMIM term:
PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS
Alternative terms:

(∗) Location:
7p15.2  
(†) Associated OMIM genes:
HOXA13  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/89j0bb1b