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bn:16361248n
Noun Concept
Categories: Autosomal dominant disorders, Abnormal clinical and laboratory findings for blood, Cytoskeletal defects
EN
Pelger-Huet anomaly  Pelger–Huët anomaly  PELGER-HUET ANOMALY; PHA  Pelger-Huët anomaly  Pelger–Huet anomaly
EN
Pelger–Huët anomaly is a blood laminopathy associated with the lamin B receptor, wherein several types of white blood cells have nuclei with unusual shape and unusual structure. Wikipedia
Definitions
Relations
Sources
EN
Pelger–Huët anomaly is a blood laminopathy associated with the lamin B receptor, wherein several types of white blood cells have nuclei with unusual shape and unusual structure. Wikipedia
Human disease Wikidata
IS A
rare disease
hematologic disease
GENETIC ASSOCIATION
lamin B receptor
HEALTH SPECIALTY
hematology
Wikipedia
EN
Pelger–Huët anomaly
Wikidata
EN
Pelger-Huet anomaly
Wikipedia Redirections
EN
Pelger-Huet anomaly, Pelger-Huët anomaly, Pelger–Huet anomaly, Pseudo-Pelger-Huet nucleus, Pseudo-Pelger-Huët anomaly, pseudo-Pelger–Huët anomaly, Pseudo Pelger-Huët anomaly, pseudo Pelger–Huët anomaly
Wikidata Alias
EN
PELGER-HUET ANOMALY, PELGER-HUET ANOMALY; PHA, PHA

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