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Autosomal Recessive Osteopetrosis 2

Disease ID: disease_node_17387

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DbxrefGARD:4157, MIM:259710
SubclassofDOID_13533, DOID_0050737
Data SourceDOID
SynonymsOPTB2, mild autosomal recessive form osteopetrosis, osteoclast-poor osteopetrosis
Doid Labelautosomal recessive osteopetrosis 2
Doid DescriptionAn osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the TNFSF11 gene on chromosome 13q14.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_17387
Doid IdDOID_0110943
LabelAutosomal Recessive Osteopetrosis 2