Preferred Name | Dentin dysplasia | |
Synonyms |
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Definitions |
This is a bundled term as dentin dysplasia is composed of short roots with pointed ends and taurodontism and intrapulpal calcifications. This term designates a genetic condition, and an Element of Morphology rending its utilization sometimes confusing. The condition is characterized by multiple dental anomalies that affect both deciduous and permanent dentitions. It can exist in isolation or be associated with other signs and symptoms of various syndromes. |
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ID |
http://purl.obolibrary.org/obo/HP_0033784 |
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comment |
This term designates a genetic condition, and an Element of Morphology rending its utilization sometimes confusing. The condition is characterized by multiple dental anomalies that affect both deciduous and permanent dentitions. It can exist in isolation or be associated with other signs and symptoms of various syndromes. |
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dc_date |
2021-05-07T10:38:57Z |
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definition |
This is a bundled term as dentin dysplasia is composed of short roots with pointed ends and taurodontism and intrapulpal calcifications. |
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has_obo_namespace |
human_phenotype |
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id |
HP:0033784 |
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label |
Dentin dysplasia |
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notation |
HP:0033784 |
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prefLabel |
Dentin dysplasia |
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terms_creator | ||
treeView | ||
subClassOf |