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bn:04810822n
Noun Named Entity
JA
No term available
EN
A Meckel syndrome that has material basis in an autosomal recessive mutation of NPHP3 on chromosome 3q22.1. Wikidata
Relations
Sources
IS A
希少疾患
メッケル・グルーバー症候群
GENETIC ASSOCIATION
EN
NPHP3

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