MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS; MCPH2

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Summary

Literature (0)

MIM:604317 - MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS; MCPH2

Xenbase Genes: wdr62

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011435 - microcephaly 2, primary, autosomal recessive, with or without cortical malformations
MONDO:0016660 - autosomal recessive primary microcephaly

MONDO:0011435 - microcephaly 2, primary, autosomal recessive, with or without cortical malformations

MONDO:0016660 - autosomal recessive primary microcephaly