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Q31814856-BCC1ED26-605E-4201-A1C3-911F8C203CEF
Q31814856-BCC1ED26-605E-4201-A1C3-911F8C203CEF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q31814856-BCC1ED26-605E-4201-A1C3-911F8C203CEF
Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia.
P2860
Q31814856-BCC1ED26-605E-4201-A1C3-911F8C203CEF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q31814856-BCC1ED26-605E-4201-A1C3-911F8C203CEF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2718929b43a1271ec03de03763e5c05c8e9162d6
P2860
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10