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DOID:0110054 - amelogenesis imperfecta type 1A
Disease Ontology Definition:An amelogenesis imperfecta that has material basis in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32.
Synonyms: AI1A, amelogenesis imperfecta hypoplastic type IA, amelogenesis imperfecta type IA,
Xenbase Genes : lamb3
MONDO:0007094 - amelogenesis imperfecta type 1A |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
amelogenesis imperfecta (is_a)