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Q24676461-0F9F8F9F-1F86-4121-AA11-354D704F6D9C
Q24676461-0F9F8F9F-1F86-4121-AA11-354D704F6D9C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676461-0F9F8F9F-1F86-4121-AA11-354D704F6D9C
Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1)
P2860
Q24676461-0F9F8F9F-1F86-4121-AA11-354D704F6D9C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676461-0F9F8F9F-1F86-4121-AA11-354D704F6D9C
rank
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type
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Statement
wasDerivedFrom
849deea730a833aa249295f76a8b652d914cdb17
P2860
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.