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bn:16900268n
Noun Concept
NL
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
ziekte
zeldzame ziekte
brachydactyly
GENETIC ASSOCIATION
PITX1

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