OBO ID: DOID:0110062 |
Term Name: | amelogenesis imperfecta hypomaturation type 2A4 | Search Ontology: | |
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Synonyms: |
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Definition: | An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21. https://www.ncbi.nlm.nih.gov/pubmed/22901946 | ||
References: |
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Ontology: | Human Disease ( DOID:0110062 ) |
OTHER amelogenesis imperfecta hypomaturation type 2A4 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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ODAPH | Amelogenesis imperfecta, type IIA4 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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