All diseases

OMIM ID
308700
OMIM term:
KALLMANN SYNDROME 1; KAL1
Alternative terms:
KMS
HYPOGONADOTROPIC HYPOGONADISM AND ANOSMIA; HHA
DYSPLASIA OLFACTOGENITALIS OF DE MORSIER
ANOSMIC HYPOGONADISM
(∗) Location:
Xp22.31  
(†) Associated OMIM genes:
KAL1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/xv2jht3l