All diseases

OMIM ID
233400
OMIM term:
PERRAULT SYNDROME; PRLTS
Alternative terms:
OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS
GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS
(∗) Location:
5q23.1  
(†) Associated OMIM genes:
HSD17B4  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/l43cw5de