Microcephaly 14, primary, autosomal recessive

MONDO:0014623

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the SASS6 gene.

Also known as: SASS6 autosomal recessive primary microcephaly, autosomal recessive primary microcephaly caused by mutation in SASS6, microcephaly 14, primary, autosomal recessive, MCPH14

0 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Neurodevelopmental disorder (147) Human disease (14) Hereditary neurological disease (6) Autosomal recessive disease (4) Microcephaly (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.