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
1 clinical trial for this condition and its sub-types.
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Disease
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Hereditary disease
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Human disease
(14)
Chromosomal disorder
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Developmental defect during embryogenesis
(8)
Congenital limb malformation
(3)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 17 disorder
(0)
Disease by developmental or physiological process
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