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Summary Literature (0)
DOID:0111722 - amelogenesis imperfecta type 3C

Disease Ontology Definition:An amelogenesis imperfecta type 3 that is characterized by hypocalcified enamel in both the primary and secondary dentition and that has_material_basis_in homozygous mutation in the RELT gene on chromosome 11q13.

Synonyms: AI3C, amelogenesis imperfecta type IIIC, autosomal recessive amelogenesis imperfecta hypocalcification type,

Xenbase Genes :



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a)