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DOID:0110052 - amelogenesis imperfecta type 1B
Disease Ontology Definition:An amelogenesis imperfecta that has material basis in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13.
Synonyms: AI1B, AIH2, amelogenesis imperfecta type IB, autosomal dominant hypoplastic local amelogenesis imperfecta, hereditary localized enamel hypoplasia,
Xenbase Genes : enam
MONDO:0007092 - amelogenesis imperfecta type 1B |
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)