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Microcephaly 17, primary, autosomal recessive

MONDO:0014908

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

Also known as: CIT autosomal recessive primary microcephaly, MCPH17, autosomal recessive primary microcephaly caused by mutation in CIT, autosomal recessive primary microcephaly caused by mutation in cit, cit autosomal recessive primary microcephaly, microcephaly 17, primary, autosomal recessive, microcephaly 17, primary, autosomal recessive; MCPH17

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

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Human disease (14) Hereditary neurological disease (5) Autosomal recessive disease (4) Microcephaly (3) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0)

Trials to join now! 12 Not yet recruiting 5 Not yet finished but already full! 2 Completed 4

Microcephaly 17, primary, autosomal recessive

Broader categories

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