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ADAMTS13

—ADAM Metallopeptidase With Thrombospondin Type 1 Motif 13

Chromosome: 9

Location: 9:133414358-133459402

OMIM: 604134

Ensembl: ENSG00000160323

Official·OMIM:604134 Official·ENSG00000160323

Encodes ADAMTS13 metalloproteinase. Mutations cause congenital TTP.

Treatment Roadmap — ADAMTS13

Preclinical

Phase 1

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Congenital Thrombotic Thrombocytopenic Purpura

Autosomal RecessivePrevalence: 1/1000000hematologic

Official·OMIM:274150 Official·ORPHA93585

Summary

Clinical Trial

Approved Therapy

Registered Variant