Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:614559 - INFANTILE CEREBELLAR-RETINAL DEGENERATION; ICRD

Xenbase Genes: aco2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013802 - infantile cerebellar-retinal degeneration

Disease Ontology (DO):
DOID:0050883 - infantile cerebellar-retinal degeneration