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Q21202953-18220E4D-FF82-49F4-80F0-B2946DB7686B
Q21202953-18220E4D-FF82-49F4-80F0-B2946DB7686B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21202953-18220E4D-FF82-49F4-80F0-B2946DB7686B
Cone rod dystrophies
P2860
Q21202953-18220E4D-FF82-49F4-80F0-B2946DB7686B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21202953-18220E4D-FF82-49F4-80F0-B2946DB7686B
rank
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wasDerivedFrom
06b03f3f642d0e9119204dc8826f66e3bdc4f55b
P2860
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation.