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Summary Literature (0)
OMIM:119800 - CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY; CCF


Xenbase Genes: pitx1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007342 - clubfoot
MONDO:0016046 - familial clubfoot with or without associated lower limb anomalies
MONDO:0017382 - familial clubfoot due to 5q31 microdeletion
MONDO:0017383 - familial clubfoot due to PITX1 point mutation

Disease Ontology (DO):
DOID:11836 - clubfoot