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7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pilocytic astrocytoma
Lethal congenital contracture syndrome type 2

BRAF ERBB3
FGFR1
KIAA1549
KRAS
NTRK2
RAF1
SRGAP3


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Pilocytic astrocytoma
BRAF FGFR1 KIAA1549 KRAS NTRK2 RAF1
SRGAP3
Lethal congenital contracture syndrome type 2
ERBB3



Pilocytic astrocytoma
Lethal congenital contracture syndrome type 2

Synonym(s):
(no synonyms)

Synonym(s):
- LCCS2
- Multiple contracture syndrome, Israeli-Bedouin type

Classification (Orphanet):
(no data available)
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:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.