All diseases

OMIM ID
227200
OMIM term:
EUNUCHOIDISM, FAMILIAL HYPOGONADOTROPIC
Alternative terms:

(∗) Location:
8p21.2  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Gnrh1  

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* quick link - http://q.sanger.ac.uk/35a0v1la