All diseases

OMIM ID
249000
OMIM term:
MECKEL SYNDROME, TYPE 1; MKS1
Alternative terms:
MECKEL-GRUBER SYNDROME, TYPE 1
MECKEL SYNDROME; MKS
MES
DYSENCEPHALIA SPLANCHNOCYSTICA
GRUBER SYNDROME
MECKEL-GRUBER SYNDROME
(∗) Location:
17q22  
(†) Associated OMIM genes:
MKS1  
(‡) Associated MGI genes:
Mks1  

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* quick link - http://q.sanger.ac.uk/mk9ykr7z