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Congenital factor XII deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Nodulosis-arthropathy-osteolysis syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
Congenital factor XII deficiency
Nodulosis-arthropathy-osteolysis syndrome

F12
(UniProt - OMIM)
 MMP14
(UniProt - OMIM)
MMP2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F12
(0.52)
MMP14


Citations in the biomedical literature:


Congenital factor XII deficiency
F12
Nodulosis-arthropathy-osteolysis syndrome
MMP14 MMP2



Congenital factor XII deficiency
Nodulosis-arthropathy-osteolysis syndrome

Synonym(s):
- Congenital Hageman factor deficiency
Synonym(s):
- Multicentric osteolysis - nodulosis - arthropathy
- NAO syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.