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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
Hemolytic anemia due to adenylate kinase deficiency

IDH1 AK1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
IDH1
(0.49)
AK1



Citations in the biomedical literature:


Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
IDH1
Hemolytic anemia due to adenylate kinase deficiency
AK1



Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
Hemolytic anemia due to adenylate kinase deficiency

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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.