Human Disease and Mouse Model Detail
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Human Disease
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Amelogenesis Imperfecta, Hypomaturation Type, Iia3; AI2A3
OMIM ID: 613211
Human Phenotype Ontology associations
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Synonyms
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Amelogenesis Imperfecta
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Disease is associated/modeled with this Gene or a homolog. More... |
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WDR72*
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Wdr72*
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View 1 model
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HomoloGene and HGNC
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References
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Disease References using Mouse Models (1)
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Mouse Models
Human Disease Modeled: Amelogenesis Imperfecta, Hypomaturation Type, Iia3; AI2A3
Associated Mouse Gene:
Wdr72
Analysis Tools