All diseases

OMIM ID
608747
OMIM term:
INSULIN-LIKE GROWTH FACTOR I DEFICIENCY
Alternative terms:
IGF1 DEFICIENCY
GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION
(∗) Location:
12q23.2  
(†) Associated OMIM genes:
IGF1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/fhnqib03