All diseases

OMIM ID
256050
OMIM term:
ATELOSTEOGENESIS, TYPE II; AOII
Alternative terms:
AO2
NEONATAL OSSEOUS DYSPLASIA I DE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED
(∗) Location:
5q32  
(†) Associated OMIM genes:
SLC26A2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/84gs5r6n