All diseases

OMIM ID
154780
OMIM term:
MARSHALL SYNDROME; MRSHS
Alternative terms:

(∗) Location:
1p21.1  
(†) Associated OMIM genes:
COL11A1  
(‡) Associated MGI genes:
Col11a1  

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* quick link - http://q.sanger.ac.uk/xs9rxvrr