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Microcephaly 7, primary, autosomal recessive

rare

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

Identifiers
MONDO:0012989 OMIM:612703
Causal genes
STIL
Part of
Autosomal recessive primary microcephaly
Also known as
autosomal recessive primary microcephaly caused by mutation in STIL · MCPH7 · STIL autosomal recessive primary microcephaly

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