Search Ontology:
Human Disease
amelogenesis imperfecta type 1H
- Term ID
- DOID:0110064
- Synonyms
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- AI1H
- amelogenesis imperfecta type IH
- 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)
- References
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- ICD10CM:K00.5
- MIM:616221
- Ontology
- Human Disease ( DOID:0110064 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models