/factor XIII, A subunit, deficiency of

factor XIII, A subunit, deficiency of

Rare Disease

MONDO:0013187

Also Known As

factor XIII, A subunit, deficiency offactor XIIIA deficiencyhereditary factor XIII A subunit deficiencyhereditary factor XIII alpha subunit deficiencyhereditary factor XIII type II deficiency

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

F13A1 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:613225 ↗

GARD

GARD:15633 ↗

Related Diseases

factor VII and Factor VIII, combined deficiency of

MONDO:0007595

Rare

platelet-type bleeding disorder 16

MONDO:0008552

Rare

hypoplasminogenemia

MONDO:0009009

Rare

Ehlers-Danlos syndrome, fibronectinemic type

MONDO:0009158

Rare

factor V and factor VIII, combined deficiency of, type 1

MONDO:0009206

Rare

congenital factor V deficiency

MONDO:0009210

Rare

← Back to All Diseases