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Summary Literature (0)
MIM:300000 - OPITZ GBBB SYNDROME; GBBB

Xenbase Genes: mid1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010222 - anatomical line between pupils
MONDO:0017138 - Opitz G/BBB syndrome

Disease Ontology (DO):
DOID:0050780 - obsolete Opitz-GBBB syndrome
DOID:0080697 - Opitz GBBB syndrome