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Summary Literature (0)
DOID:0110062 - amelogenesis imperfecta hypomaturation type 2A4

Disease Ontology Definition:An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21.

Synonyms: AI2A4, amelogenesis imperfecta hypomaturation type IIA4, amelogenesis imperfecta type IIA4,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013906 - amelogenesis imperfecta hypomaturation type 2A4


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 recessive disease (is_a)