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Congenital alpha2 antiplasmin deficiency
1 OMIM reference -
1 associated gene
17 connected diseases
No signs/symptoms info
Disease Type of connection
Hypoplasminogenemia
Ligneous conjunctivitis
Autosomal dominant severe congenital neutropenia
Cyclic neutropenia
Hereditary chronic pancreatitis
Recurrent Neisseria infections due to factor D deficiency
CADDS
Fibronectin glomerulopathy
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Congenital factor XI deficiency
Congenital factor XIII deficiency
Quebec platelet disorder
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
SERPINF2 P08697613168
No signs/symptoms info available.