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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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Skeletal dysplasia
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Spondylometaphyseal dysplasia
SBDS-related severe neonatal spondylometaphyseal dysplasia
rare
Identifiers
MONDO:0850096
Orphanet:622934
Part of
Spondylometaphyseal dysplasia
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