All diseases

OMIM ID
146255
OMIM term:
HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE; HDR
Alternative terms:
HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DYSPLASIA SYNDROME; HDRS
BARAKAT SYNDROME
NEPHROSIS, NERVE DEAFNESS, AND HYPOPARATHYROIDISM
(∗) Location:
10p14  
(†) Associated OMIM genes:
GATA3  
(‡) Associated MGI genes:
Gata3  

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* quick link - http://q.sanger.ac.uk/vqdr8017