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

FADD
(UniProt - OMIM)
 FGFR1
(UniProt - OMIM)
FGF3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FGF3
(0.52)
FGFR1


Citations in the biomedical literature:


Oculootodental syndrome
FADD FGF3
Myeloid neoplasm associated with FGFR1 rearrangement
FGFR1



Oculootodental syndrome
Myeloid neoplasm associated with FGFR1 rearrangement

Synonym(s):
- OOD
Synonym(s):
- 8p11 myeloproliferative syndrome
- Stem cell leukemia/lymphoma
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
(no data available)
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.