Any Seckel syndrome in which the cause of the disease is a mutation in the CENPJ gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
Seckel syndrome 1
MONDO:0008869
intrauterine growth retardation with increased mitomycin c sensitivity
MONDO:0010900
Seckel syndrome 2
MONDO:0011715
microcephaly 6, primary, autosomal recessive
MONDO:0012029
Seckel syndrome 5
MONDO:0013443
Seckel syndrome 6
MONDO:0013871