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Summary Literature (0)
MIM:149000 - KLIPPEL-TRENAUNAY-WEBER SYNDROME

Xenbase Genes: aggf1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007864 - angioosteohypertrophic syndrome

Disease Ontology (DO):
DOID:2926 - Klippel-Trenaunay syndrome