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bn:02888840n
Noun Concept
SYL
No term available
EN
Chondrodysplasia Blomstrand is a rare genetic disorder characterized by a mutation of the parathyroid hormone receptor, leading to the absence of a functional PTHR1. Wikipedia
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Sources
IS A
EN
rare disease
EN
osteochondrodysplasia
GENETIC ASSOCIATION
EN
Parathyroid hormone 1 receptor

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