OBO ID: DOID:0110064 |
Term Name: | amelogenesis imperfecta type 1H | Search Ontology: | |
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Definition: | An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the integrin beta-6 gene (ITGB6) on chromosome 2q24. (2) | ||
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Ontology: | Human Disease ( DOID:0110064 ) |
OTHER amelogenesis imperfecta type 1H PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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