All diseases

OMIM ID
602875
OMIM term:
ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM ST. HELENA DYSPLASIA, INCLUDED
Alternative terms:

(∗) Location:
9p13.3  
(†) Associated OMIM genes:
NPR2  
(‡) Associated MGI genes:
Npr2  

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* quick link - http://q.sanger.ac.uk/5pl1m5wh