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bn:16872020n
Noun Concept
SYL
No term available
EN
Eiken syndrome is a rare autosomal bone dysplasia with a skeletal phenotype which has been described in a unique consanguineous family, where it segregates as a recessive trait. Wikipedia
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Sources
IS A
EN
disease
EN
rare disease
EN
autosomal recessive disease
GENETIC ASSOCIATION
EN
Parathyroid hormone 1 receptor

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