amelogenesis imperfecta type 1G (Q27164432)
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amelogenesis imperfecta that has material basis in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24
- AI1G
- AIGFS
- ERS
- amelogenesis imperfecta and gingival fibromatosis syndrome
- amelogenesis imperfecta hypoplastic with nephrocalcinosis
- amelogenesis imperfecta type IG
- enamel-renal syndrome
- enamel-renal-gingival syndrome
- Amelogenesis Imperfecta, Hypoplastic, With Nephrocalcinosis
- AMELOGENESIS IMPERFECTA, TYPE IG
- Amelogenesis imperfecta-nephrocalcinosis syndrome
- AMELOGENESIS IMPERFECTA, TYPE IG; AI1G
- Enamel-renal syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | amelogenesis imperfecta type 1G |
amelogenesis imperfecta that has material basis in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24 |
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Sitelinks
Wikipedia(1 entry)
- enwiki Enamel-renal syndrome