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Congenital prekallikrein deficiency
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital high-molecular-weight kininogen deficiency
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Congenital factor XII deficiency
Hereditary angioedema type 3
Primary sclerosing cholangitis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KLKB1 P03952229000
No signs/symptoms info available.