Metadata | |
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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 |