Familial clubfoot due to 17q23.1q23.2 microduplication
MONDO:001332917q23.1-q23.2 microduplication is a newly described cause of familial isolated clubfoot.
Also known as: hereditary clubfoot due to 17q23.1-q23.2 microduplication, chromosome 17q23.1-q23.2 DUPLICATION syndrome
7 clinical trials for this condition and its sub-types.
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Disease
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Hereditary disease
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Human disease
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Chromosomal disorder
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Developmental defect during embryogenesis
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Congenital limb malformation
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Disease of genetic or genomic mechanism
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Autosomal anomaly
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Chromosome 17 disorder
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Disease by developmental or physiological process
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