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Congenital factor XIII deficiency
2 OMIM references -
2 associated genes
18 connected diseases
No signs/symptoms info
Disease Type of connection
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Fibronectin glomerulopathy
22q11.2 deletion syndrome
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Multiple endocrine neoplasia type 1
Spondylocarpotarsal synostosis
Cerebral sinovenous thrombosis
Congenital alpha2 antiplasmin deficiency
Congenital factor II deficiency
Synonym(s):
- Fibrin-stabilizing factor deficiency
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:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
F13A1 P00488134570
F13B P05160134580
No signs/symptoms info available.