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DOID:0110057 - amelogenesis imperfecta type 2A1
Disease Ontology Definition:An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the kallikrein-4 gene (KLK4) on chromosome 19q13.
Synonyms: AI2A1, amelogenesis imperfecta pigmented hypomaturation type 1, amelogenesis imperfecta type IIA1,
Echinobase Genes :
MIM:204700 - amelogenesis imperfecta, hypomaturation type, iia1; ai2a1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee