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amelogenesis imperfecta hypomaturation type 2A5 | RareConnect | RareConnect.io

/amelogenesis imperfecta type 2

/amelogenesis imperfecta hypomaturation type 2A5

amelogenesis imperfecta hypomaturation type 2A5

Rare Disease

MONDO:0014385

Also Known As

AI2A5SLC24A4 amelogenesis imperfectaamelogenesis imperfecta caused by mutation in SLC24A4amelogenesis imperfecta hypomaturation type IIA5amelogenesis imperfecta type IIA5amelogenesis imperfecta, type IIA5amelogenesis imperfecta, hypomaturation type, IIA5

Definition

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the SLC24A4 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615887 ↗

GARD

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