Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Skeletal dysplasia - orofacial anomalies as a "rare disease".
Source - Orphanet
Skeletal dysplasia - orofacial anomalies: Introduction
Symptoms of Skeletal dysplasia - orofacial anomalies: see symptoms of Skeletal dysplasia - orofacial anomalies
Treatments for Skeletal dysplasia - orofacial anomalies:
see treatments for Skeletal dysplasia - orofacial anomalies
Main name of condition: Skeletal dysplasia - orofacial anomalies
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