(Q27674801)
English
amelogenesis imperfecta type 2A1
amelogenesis imperfecta that has material basis in homozygous mutation in the kallikrein-4 gene (KLK4) on chromosome 19q13
- AI2A1
- amelogenesis imperfecta pigmented hypomaturation type 1
- amelogenesis imperfecta type IIA1
- AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1
- Amelogenesis Imperfecta, Pigmented Hypomaturation Type, 1
- Amelogenesis imperfecta pigmented hypomaturation type
- AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1; AI2A1
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