microcephaly 9, primary, autosomal recessive

Rare Disease

MONDO:0013923

Also Known As

CEP152 autosomal recessive primary microcephalyautosomal recessive primary microcephaly caused by mutation in CEP152microcephaly 9, primary, autosomal recessiveMCPH9

Definition

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CEP152 gene.

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Associated Genes

CEP152 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614852 ↗

GARD

GARD:15855 ↗

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