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bn:06294019n
Noun Named Entity
JA
Hoyeraal-Hreidarsson症候群
EN
Hoyeraal–Hreidasson syndrome is a very rare multisystem X-linked recessive disorder characterized by excessively short telomeres and is considered a severe form of dyskeratosis congenita. Wikipedia
Relations
Sources
IS A
病気
希少疾患
症候群
X連鎖劣性
先天性角化異常症
GENETIC ASSOCIATION
テロメラーゼ逆転写酵素
ジスケリン
EN
Poly(A)-specific ribonuclease
EN
TINF2
EN
ACD
HEALTH SPECIALTY
遺伝医学
Wikidata
JA
Hoyeraal-Hreidarsson症候群

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