| Metadata | |
|---|---|
| ID | DOID:0110062 |
| Name | amelogenesis imperfecta hypomaturation type 2A4 |
| Definition | An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21. https://www.ncbi.nlm.nih.gov/pubmed/22901946 |
| Xrefs | |
| Synonyms |
AI2A4 [EXACT] amelogenesis imperfecta hypomaturation type IIA4 [EXACT] amelogenesis imperfecta type IIA4 [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |