amelogenesis imperfecta type 1F

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Summary

Literature (0)

DOID:0110065 - amelogenesis imperfecta type 1F

Disease Ontology Definition:An amelogenesis imperfecta that has material basis in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13.

Synonyms: AI1F, amelogenesis imperfecta hypoplastic type IF, amelogenesis imperfecta type IF,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ambn

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014560 - amelogenesis imperfecta type 1F

MONDO:0014560 - amelogenesis imperfecta type 1F

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)