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bn:16900268n
Noun Concept
SYL
No term available
EN
Liebenberg Syndrome is a rare autosomal genetic disease that involves a deletion mutation upstream of the PITX1 gene, which is one that's responsible for the body's organization, specifically in forming lower limbs. Wikipedia
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IS A
EN
disease
EN
rare disease
EN
brachydactyly
GENETIC ASSOCIATION
EN
PITX1

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