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persistent hyperplastic primary vitreous, autosomal dominant | RareConnect | RareConnect.io

/persistent hyperplastic primary vitreous

/persistent hyperplastic primary vitreous, autosomal dominant

persistent hyperplastic primary vitreous, autosomal dominant

Rare Disease

MONDO:0012653

Also Known As

PHPVADpersistent hyperplastic primary vitreous, autosomal dominant

Patient-Friendly Information

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External Resources

OMIM

OMIM:611308 ↗

GARD

Related Diseases

persistent hyperplastic primary vitreous, autosomal recessive

MONDO:0009097

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