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(HPO:0005652) | Cortical sclerosis | 1 / 7739 | ||||
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(OMIM) | Dense long bones | 2 / 7739 | ||||
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(OMIM) | Dense maxillary and mandibular alveoli | 1 / 7739 | ||||
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(OMIM) | Narrow or occluded marrow spaces and thick cortices | 1 / 7739 | ||||
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(OMIM) | Radicular dentin dysplasia | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(HPO:0011060) | Dentinogenesis imperfecta limited to primary teeth | 3 / 7739 |