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Summary Literature (1)
MIM:248200 - STARGARDT DISEASE 1; STGD1

Xenbase Genes: abca4, cngb3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009549 - severe early-childhood-onset retinal dystrophy

Disease Ontology (DO):
DOID:0050817 - Stargardt disease