All diseases

OMIM ID
251200
OMIM term:
MICROCEPHALY 1, PRIMARY, AUTOSOMAL RECESSIVE; MCPH1
Alternative terms:
PREMATURE CHROMOSOME CONDENSATION WITH MICROCEPHALY AND MENTAL RETARDATION
PREMATURE CHROMOSOME CONDENSATION SYNDROME
PCC SYNDROME
(∗) Location:
8p23.1  
(†) Associated OMIM genes:
MCPH1  
(‡) Associated MGI genes:
Mcph1  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/wuopf4og