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Q35200261-37D6A4DC-24C7-4043-9912-84FBE36C5638
Q35200261-37D6A4DC-24C7-4043-9912-84FBE36C5638
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35200261-37D6A4DC-24C7-4043-9912-84FBE36C5638
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.
P2860
Q35200261-37D6A4DC-24C7-4043-9912-84FBE36C5638
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35200261-37D6A4DC-24C7-4043-9912-84FBE36C5638
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
bb46f5f9bbd81bf9522877ff8b2d1ea1568229db
P2860
X-linked retinitis pigmentosa.