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familial clubfoot due to PITX1 point mutation | RareConnect | RareConnect.io

/familial clubfoot due to PITX1 point mutation

familial clubfoot due to PITX1 point mutation

Rare Disease

MONDO:0017383

Also Known As

hereditary clubfoot due to PITX1 point mutation

Patient-Friendly Information

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External Resources

Orphanet

Orphanet:293150 ↗

GARD

Related Diseases

familial clubfoot due to 5q31 microdeletion

MONDO:0017382

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