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Autosomal Domit Severe Congenital Neutropenia

Disease ID: disease_node_18061

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DbxrefGARD:9558, ORDO:486
SubclassofDOID_0050736, DOID_0050590
Data SourceDOID
Doid Labelautosomal domit severe congenital neutropenia
Doid DescriptionA severe congenital neutropenia that has_material_basis_in heterozygous mutation of an autosomal gene.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_18061
Doid IdDOID_0112130
Disease Has Basis InHP_0001197
LabelAutosomal Domit Severe Congenital Neutropenia