All diseases

OMIM ID
262700
OMIM term:
PITUITARY HORMONE DEFICIENCY, COMBINED, 4; CPHD4
Alternative terms:
PITUITARY HORMONE DEFICIENCY, COMBINED, WITH OR WITHOUT CEREBELLAR DEFECTS
SHORT STATURE, PITUITARY AND CEREBELLAR DEFECTS, AND SMALL SELLA TURCICA
(∗) Location:
1q25.2  
(†) Associated OMIM genes:
LHX4 LHX4/IGHG1 FUSION GENE, INCLUDED  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/wqgx1bnv