/inherited prekallikrein deficiency

inherited prekallikrein deficiency

Rare Disease

MONDO:0012901

Also Known As

congenital prekallikrein deficiencyfletcher factor (prekallikrein) deficiencyhereditary prekallikrein deficiencyFletcher Factor deficiencyPKK deficiencyprekallikrein deficiencyprekallikrein deficiency, congenital

Definition

An instance of prekallikrein deficiency that is caused by an inherited modification of the individual's genome.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

KLKB1 ↗

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

External Resources

Related Diseases

inherited bleeding disorder, platelet-type

MONDO:0000009

Rare

factor XIII deficiency

MONDO:0002241

Rare

factor VII deficiency

MONDO:0002244

Rare

factor X deficiency

MONDO:0002247

Rare

purpura

MONDO:0002610

Rare

vascular hemostatic disease

MONDO:0003159

Rare

← Back to All Diseases

inherited prekallikrein deficiency

Also Known As

Definition

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases