Details of Disease | DrugMAP

General Information of Disease (ID: DIS10DE3)

Disease Name	Microcephaly 16, primary, autosomal recessive
Synonyms	microcephaly 16, primary, autosomal recessive; microcephaly 16, primary, autosomal recessive; MCPH16; MCPH16
Disease Hierarchy	DIS29IE3: Autosomal recessive primary microcephaly DIS10DE3: Microcephaly 16, primary, autosomal recessive
Disease Identifiers	MONDO ID MONDO_0014730 UMLS CUI C4225249 OMIM ID 616681 MedGen ID 898705

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ANKLE2	OTHCYR6Y	Strong	Autosomal recessive	[1]
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References

1	A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases. Cell. 2014 Sep 25;159(1):200-214. doi: 10.1016/j.cell.2014.09.002.