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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Congenital nervous system disorder
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Congenital vitreoretinal dysplasia
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Persistent hyperplastic primary vitreous
Persistent hyperplastic primary vitreous, autosomal dominant
rare
Identifiers
MONDO:0012653
OMIM:611308
Part of
Persistent hyperplastic primary vitreous
Also known as
PHPVAD
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