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bn:03840398n
Noun Concept
JA
メッケル・グルーバー症候群  メッケルグーバ症候群  メッケル症候群
EN
Meckel-Gruber syndrome is a rare, lethal ciliopathic genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations, polydactyly, hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios. Wikipedia
Relations
Sources
IS A
希少疾患
優性
症候群
繊毛病
HAS KIND
EN
Meckel syndrome type 7
EN
Grauhan syndrome
GENETIC ASSOCIATION
EN
MKS1
HEALTH SPECIALTY
遺伝医学
NAMED AFTER
ヨハン・フリードリッヒ・メッケル
EN
Georg Benno Gruber
Wikidata
JA
メッケル・グルーバー症候群
Wikipedia Translations
JA
メッケルグーバ症候群, メッケル症候群

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