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Summary Literature (0)
MIM:613735 - BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD

Xenbase Genes: nfia

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013396 - chromosome 1p32-p31 deletion syndrome

Disease Ontology (DO):
DOID:0060409 - NFIA-related disorder