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DOID:0110945 - autosomal recessive osteopetrosis 6
Disease Ontology Definition:An osteopetrosis characterized by autosomal recessive inheritance of that has_material_basis_in mutation in the PLEKHM1 gene on chromosome 17q21.31.
Synonyms: OPTB6, autosomal recessive osteopetrosis intermediate form,
Xenbase Genes : clcn7, tcirg1, plekhm1
MONDO:0012679 - autosomal recessive osteopetrosis 6 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee