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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
12 associated genes
No signs/symptoms info
Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
Gliosarcoma

IDH1 EGFR
FGFR1
FGFR3
IDH1
LZTR1
MGMT
NFKBIA
PPARG
SEPT14
TACC1
TACC3
TP53


COMMON
GENES
IDH1



Citations in the biomedical literature:


Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
IDH1
Gliosarcoma
EGFR FGFR1 FGFR3 LZTR1 MGMT
NFKBIA PPARG SEPT14 TACC1 TACC3 TP53



Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
Gliosarcoma

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

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

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

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

No signs/symptoms info available.