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Standards Ontologies Notations
amelogenesis imperfecta

Summary
Definition
A dental enamel hypoplasia characterized by abnormal enamel formation.
Super Class
dental enamel hypoplasia
Disease Ontology
DOID:2187
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
56975 FAM20C FAM20C golgi associated secretory pathway kinase
Displaying 1 entry
Gene ID Gene Symbol Description Source
80752 Fam20c FAM20C, golgi associated secretory pathway kinase
Displaying 1 entry
Gene ID Gene Symbol Description Source
42784 CG31145 uncharacterized protein
Displaying 1 entry
Gene ID Gene Symbol Description Source
181616 famk-1 Extracellular serine/threonine protein kinase CeFam20
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024