| ADR Ontology |
| ADR Term |
Tooth hypoplasia |
| ADR ID |
BADD_A04343 |
| ADR Hierarchy |
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| Description |
An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors. | A type of developmental disturbance of AMELOGENESIS involving permanent INCISORS and first permanent MOLARS. It is characterized by asymmetrical enamel defects with severe hypomineralization. [MeSH] |
| MedDRA Code |
10044041 |
| MeSH ID |
D003744
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ADR Severity Grade (FAERS)
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ADR Severity Grade (CTCAE)
|
Not Available
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| Synonym |
| Dental development impaired | Development dental impaired | Dysplasia tooth | Enamel hypoplasia | Hypoplasia enamel | Hypoplasia tooth | Odontogenesis impaired | Tooth formation retarded | Tooth hypoplasia | Dental Enamel Hypoplasia | Hypoplastic Enamel | Enamel, Hypoplastic | Enamel Hypoplasia, Dental | Hypoplasia, Dental Enamel | Enamel Agenesis | Ageneses, Enamel | Agenesis, Enamel | Enamel Ageneses | Enamel Hypoplasia | Enamel Hypoplasias | Hypoplasia, Enamel | Hypoplasias, Enamel | Molar Incisor Hypomineralization | Hypomineralization, Molar Incisor |
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| ADR Related Proteins |
| Protein Name |
UniProt AC |
TTD Target ID |
| Not Available | Not Available | Not Available |
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| Drugs Leading to the ADR |
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