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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

Hunting for hidden genes behind tooth defects

Knowledge-focused Completed

This study aims to discover new genes and mutations that cause isolated forms of amelogenesis imperfecta and dentinogenesis imperfecta—inherited conditions that affect tooth enamel and dentin. Researchers are using whole exome sequencing on participants who have these tooth disor…

Phase: NA • Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused

Last updated Jul 22, 2026 00:00 UTC