Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Sclerocornea, Syndactyly, ambiguous genitalia as a "rare disease".
Source - Orphanet
Sclerocornea, Syndactyly, ambiguous genitalia: Introduction
Symptoms of Sclerocornea, Syndactyly, ambiguous genitalia: see symptoms of Sclerocornea, Syndactyly, ambiguous genitalia
Diagnostic testing: see tests for Sclerocornea, Syndactyly, ambiguous genitalia.
Misdiagnosis: see misdiagnosis and Sclerocornea, Syndactyly, ambiguous genitalia.
Treatments for Sclerocornea, Syndactyly, ambiguous genitalia:
see treatments for Sclerocornea, Syndactyly, ambiguous genitalia
Main name of condition: Sclerocornea, Syndactyly, ambiguous genitalia
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