All diseases

OMIM ID
609441
OMIM term:
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES
Alternative terms:

(∗) Location:
4q22.3  
(†) Associated OMIM genes:
BMPR1B  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/5s6sp14v