Search Ontology:
Human Disease
amelogenesis imperfecta type 1E
- Term ID
- DOID:0110058
- Synonyms
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- AIH1
- amelogenesis imperfecta hypomaturationtype with snow-capped teeth
- amelogenesis imperfecta type IE
- Definition
- An amelogenesis imperfecta that has_material_basis_in X-linked dominant mutation in the gene encoding amelogenin (AMELX). (2)
- References
-
- ICD10CM:K00.5
- MIM:301200
- Ontology
- Human Disease ( DOID:0110058 )
- is a type of
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Genes Involved
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Zebrafish Models