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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Autosomal genetic disease
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Autosomal dominant disease
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Autosomal dominant osteopetrosis
Osteopetrosis, autosomal dominant 3
rare
Identifiers
MONDO:0020848
OMIM:618107
Causal genes
PLEKHM1
Part of
Autosomal dominant osteopetrosis
Also known as
OPTA3
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