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congenital symblepharon | RareConnect | RareConnect.io

/isolated cryptophthalmia

/congenital symblepharon

congenital symblepharon

Rare Disease

MONDO:0020359

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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External Resources

Orphanet

Orphanet:98948 ↗

GARD

Related Diseases

complete cryptophthalmia

MONDO:0020360

partial cryptophthalmia

MONDO:0020361

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