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bn:02426276n
Noun Concept
Categories: DNA replication and repair-deficiency disorders, All articles needing additional references, Progeroid syndromes, Congenital disorders, Telomeropathies
EN
dyskeratosis congenita  XL-dyskeratosis congenita  Zinsser-Cole-Engman syndrome  Zinsser-Engman-Cole syndrome  Zinsser–Cole–Engman syndrome
EN
Dyskeratosis congenita, also known as Zinsser-Engman-Cole syndrome, is a rare progressive congenital disorder with a highly variable phenotype. Wikipedia
Definitions
Relations
Sources
EN
Dyskeratosis congenita, also known as Zinsser-Engman-Cole syndrome, is a rare progressive congenital disorder with a highly variable phenotype. Wikipedia
A genetic disease Wikipedia Disambiguation
Rare progressive congenital disorder with a highly variable phenotype Wikidata
A rare progressive congenital disorder with a highly variable phenotype, sometimes resembling premature aging, and typically first affecting the skin and proceeding to bone marrow failure. Wiktionary
IS A
rare disease
skin disease
dyskeratosis
HAS KIND
Revesz syndrome
Hoyeraal-Hreidarsson syndrome
HEALTH SPECIALTY
medical genetics
Wikipedia
EN
dyskeratosis congenita
Wikidata
EN
dyskeratosis congenita
Wiktionary
EN
dyskeratosis congenita
Wikipedia Redirections
EN
Dyskeratosis congenita (Zinsser-Cole-Engman syndrome), XL-dyskeratosis congenita, Zinsser-Cole-Engman syndrome, Zinsser-Engman-Cole syndrome, Zinsser–Cole–Engman syndrome

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