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Autosomal Domit Primary Microcephaly 22

Disease ID: disease_node_19302

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DbxrefMIM:617984
SubclassofDOID_0070296
Data SourceDOID
Doid Labelautosomal domit primary microcephaly 22
Doid DescriptionA primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the NCAPD3 gene on chromosome 11q25.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_19302
Doid IdDOID_0051033
LabelAutosomal Domit Primary Microcephaly 22