amelogenesis imperfecta type 1B (Q27674797)
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amelogenesis imperfecta that has material basis in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13
- AI1B
- AIH2
- amelogenesis imperfecta type IB
- autosomal dominant hypoplastic local amelogenesis imperfecta
- hereditary localized enamel hypoplasia
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | amelogenesis imperfecta type 1B |
amelogenesis imperfecta that has material basis in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13 |
|
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Identifiers
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