All diseases

OMIM ID
207410
OMIM term:
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS; ABS2
Alternative terms:
TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME
MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES
OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES
(∗) Location:
10q26.13  
(†) Associated OMIM genes:
FGFR2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/le0f1bzc