Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
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

Echinobase Genes :


MIM:
MIM:104500 - amelogenesis imperfecta, type ib; ai1b

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

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