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Atypical dentin dysplasia due to SMOC2 deficiency

MONDO:0017819

Also known as: dentin dysplasia type 1 with microdontia and shape anomalies, dentin dysplasia, type IA

2 clinical trials for this condition and its sub-types.

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Broader categories

Disease (647) Musculoskeletal system disorder (202) Hereditary disease (176) Tooth disorder (30) Mouth disorder (18) Human disease (14) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Dentin dysplasia (1) Tooth hard tissue disease (1)
Not yet recruiting 1 Completed 1
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