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Q37502202-4049A5B3-98C2-4B01-BDD6-5DC0E31362CE
Q37502202-4049A5B3-98C2-4B01-BDD6-5DC0E31362CE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37502202-4049A5B3-98C2-4B01-BDD6-5DC0E31362CE
Adamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development.
P2860
Q37502202-4049A5B3-98C2-4B01-BDD6-5DC0E31362CE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37502202-4049A5B3-98C2-4B01-BDD6-5DC0E31362CE
rank
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type
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Statement
wasDerivedFrom
e2f2fcf5349b0e3722399b4fea1c79a6f22d5d9b
P2860
Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.