| Metadata | |
|---|---|
| ID | DOID:0110061 |
| Name | amelogenesis imperfecta hypomaturation type 2A3 |
| Definition | An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene. https://www.ncbi.nlm.nih.gov/pubmed/19853237 |
| Xrefs | |
| Synonyms |
AI2A3 [EXACT] amelogenesis imperfecta hypomaturation type IIA3 [EXACT] amelogenesis imperfecta type IIA3 [EXACT] |
| Parent Relationships |