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


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

In Mondo Disease Ontology:
MONDO:0009549 - severe early-childhood-onset retinal dystrophy

Human Disease Resources: OMIM

Xenbase Genes: abca4, cngb3