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Summary Literature (0)
MIM:166600 - OSTEOPETROSIS, AUTOSOMAL DOMINANT 2; OPTA2

Xenbase Genes: clcn7

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008156 - autosomal dominant osteopetrosis 2

Disease Ontology (DO):
DOID:0110938 - autosomal dominant osteopetrosis 2