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amelogenesis imperfecta hypomaturation type 2A2 | RareConnect | RareConnect.io

/amelogenesis imperfecta type 2

/amelogenesis imperfecta hypomaturation type 2A2

amelogenesis imperfecta hypomaturation type 2A2

Rare Disease

MONDO:0012926

Also Known As

AI2A2MMP20 amelogenesis imperfectaamelogenesis imperfecta caused by mutation in MMP20amelogenesis imperfecta hypomaturation type IIA2amelogenesis imperfecta pigmented hypomaturation type 2amelogenesis imperfecta type IIA2amelogenesis imperfecta, type IIA2amelogenesis imperfecta, hypomaturation type, IIA2amelogenesis imperfecta, pigmented hypomaturation type, 2

Definition

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the MMP20 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:612529 ↗

GARD

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