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Summary Literature (1)
MIM:612948 - STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, MENTAL RETARDATION, AND DYSMORPHIC FACIAL FEATURES

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013055 - Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features