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Summary Literature (0)
DOID:0060305 - megalocornea

Disease Ontology Definition:A corneal disease that is characterized by a bilaterally enlarged corneal diameter without an increase in intraocular pressure and that has_material_basis_in mutation in the CHRDL1 gene.

Synonyms: anterior megalophthalmos, congenital anterior megalophthalmia

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009576 - medulla oblongata sulcus limitans

MIM:
MIM:249300 - MEGALOCORNEA
MIM:309300 - MEGALOCORNEA; MGC1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): corneal disease (is_a), X-linked recessive disease (is_a)