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Q42538852-19AACAD3-FE3A-49A6-AAB2-B1AF38DD2C2C
Q42538852-19AACAD3-FE3A-49A6-AAB2-B1AF38DD2C2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-19AACAD3-FE3A-49A6-AAB2-B1AF38DD2C2C
'Behr syndrome' with OPA1 compound heterozygote mutations.
P407
Q42538852-19AACAD3-FE3A-49A6-AAB2-B1AF38DD2C2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-19AACAD3-FE3A-49A6-AAB2-B1AF38DD2C2C
rank
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type
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Statement
P407
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