All diseases

OMIM ID
262190
OMIM term:
PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES
Alternative terms:
MENDENHALL SYNDROME
RABSON-MENDENHALL SYNDROME
(∗) Location:
19p13.2  
(†) Associated OMIM genes:
INSR  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/mz584n8e