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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Myeloid neoplasm associated with FGFR1 rearrangement
Nodulosis-arthropathy-osteolysis syndrome

FGFR1 MMP14
MMP2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FGFR1
(0.55)
MMP2



Citations in the biomedical literature:


Myeloid neoplasm associated with FGFR1 rearrangement
FGFR1
Nodulosis-arthropathy-osteolysis syndrome
MMP14 MMP2



Myeloid neoplasm associated with FGFR1 rearrangement
Nodulosis-arthropathy-osteolysis syndrome

Synonym(s):
- 8p11 myeloproliferative syndrome
- Stem cell leukemia/lymphoma

Synonym(s):
- Multicentric osteolysis - nodulosis - arthropathy
- NAO syndrome

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
(no data available)
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.