All diseases

OMIM ID
100800
OMIM term:
ACHONDROPLASIA; ACH
Alternative terms:

(∗) Location:
4p16.3  
(†) Associated OMIM genes:
FGFR3  
(‡) Associated MGI genes:
Acan   Fgfr3   Npr2   Pthlh   Spred2  

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* quick link - http://q.sanger.ac.uk/2l39qozp