" /> Amelogenesis imperfecta, hypomaturation type, iia6 - CISMeF





Preferred Label : Amelogenesis imperfecta, hypomaturation type, iia6;

Symbol : AI2A6;

CISMeF acronym : AI2A6;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the G protein-coupled receptor 68 gene (GPR68, 601404.0001);

Prefixed ID : #617217;

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10/05/2025


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