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Myeloid neoplasm associated with FGFR1 rearrangement
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Lethal congenital contracture syndrome type 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Myeloid neoplasm associated with FGFR1 rearrangement
Lethal congenital contracture syndrome type 2

FGFR1
(UniProt - OMIM)
 ERBB3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FGFR1
(0.63)
ERBB3


Citations in the biomedical literature:


Myeloid neoplasm associated with FGFR1 rearrangement
FGFR1
Lethal congenital contracture syndrome type 2
ERBB3



Myeloid neoplasm associated with FGFR1 rearrangement
Lethal congenital contracture syndrome type 2

Synonym(s):
- 8p11 myeloproliferative syndrome
- Stem cell leukemia/lymphoma
Synonym(s):
- LCCS2
- Multiple contracture syndrome, Israeli-Bedouin type
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.