All diseases

OMIM ID
250250
OMIM term:
CARTILAGE-HAIR HYPOPLASIA; CHH
Alternative terms:

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

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/xse11fu3