Amelogenesis Imperfecta, Type Iiic (AI3C)

Alias:

Ai3c

Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Recessive

Amelogenesis Imperfecta, Type 3c

Amelogenesis Imperfecta Type 3c

Autosomal Recessive Amelogenesis Imperfecta Hypocalcification Type

Amelogenesis Imperfecta Type Iiic

Amelogenesis Imperfecta 3c

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Amelogenesis Imperfecta, Type Iiic, also known as ai3c, is related to amelogenesis imperfecta, hypomaturation type, iia5 and amelogenesis imperfecta, type iv. An important gene associated with Amelogenesis Imperfecta, Type Iiic is RELT (RELT TNF Receptor), and among its related pathways/superpathways are GABA B receptor activation and Regulation of CFTR activity (norm and CF). Related phenotypes are yellow-brown discoloration of the teeth and amelogenesis imperfecta

Related ID：

MALACARDS：AML064

OMIM：618386

MESH：D000567