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amelogenesis imperfecta hypomaturation type 2A3 | RareConnect | RareConnect.io

/amelogenesis imperfecta type 2

/amelogenesis imperfecta hypomaturation type 2A3

amelogenesis imperfecta hypomaturation type 2A3

Rare Disease

MONDO:0013181

Also Known As

AI2A3WDR72 amelogenesis imperfectaamelogenesis imperfecta caused by mutation in WDR72amelogenesis imperfecta hypomaturation type 2A3amelogenesis imperfecta hypomaturation type IIA3amelogenesis imperfecta type IIA3amelogenesis imperfecta, type IIA3amelogenesis imperfecta, hypomaturation type, IIA3

Definition

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the WDR72 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:613211 ↗

GARD

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