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Q28280427-E6D4EC98-D5A6-4E61-AAFC-9FA0392B8AE4
Q28280427-E6D4EC98-D5A6-4E61-AAFC-9FA0392B8AE4
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Statement
http://www.wikidata.org/entity/statement/Q28280427-E6D4EC98-D5A6-4E61-AAFC-9FA0392B8AE4
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
P2860
Q28280427-E6D4EC98-D5A6-4E61-AAFC-9FA0392B8AE4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28280427-E6D4EC98-D5A6-4E61-AAFC-9FA0392B8AE4
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wasDerivedFrom
fbfacb03ec29ebd57e6aa4ad765dbefce4fdf440
P2860
Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original "Kostmann family" and a review.