All diseases

OMIM ID
224690
OMIM term:
MEIER-GORLIN SYNDROME 1; MGORS1
Alternative terms:
EAR, PATELLA, SHORT STATURE SYNDROME; EPS
MICROTIA, ABSENT PATELLAE, MICROGNATHIA SYNDROME
MEIER-GORLIN SYNDROME
(∗) Location:
1p32.3  
(†) Associated OMIM genes:
ORC1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/9yjyrka9