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Q49119860-87229EB8-E8AD-426F-AF7E-5A329ECA8DAF
Q49119860-87229EB8-E8AD-426F-AF7E-5A329ECA8DAF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49119860-87229EB8-E8AD-426F-AF7E-5A329ECA8DAF
Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature child.
P2860
Q49119860-87229EB8-E8AD-426F-AF7E-5A329ECA8DAF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49119860-87229EB8-E8AD-426F-AF7E-5A329ECA8DAF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a159f72089e8f82d9b1836ea420060044fb824b0
P2860
Cardiac abnormalities in patients with Leber's hereditary optic neuropathy.