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bn:02801991n
Noun Concept
JA
No term available
EN
Pfeiffer syndrome is a rare genetic disorder, characterized by the premature fusion of certain bones of the skull, which affects the shape of the head and face. Wikipedia
Relations
Sources
IS A
希少疾患
遺伝子疾患
EN
acrocephalosyndactylia
DIFFERENT FROM
伝染性単核球症
GENETIC ASSOCIATION
線維芽細胞増殖因子受容体1
線維芽細胞増殖因子受容体2
HEALTH SPECIALTY
リウマチ学

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