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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Spinocerebellar ataxia type 26
Acute myelomonocytic leukemia

EEF2 FLT3
SCA26 NPM1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EEF2
(0.63)
NPM1



Citations in the biomedical literature:


Spinocerebellar ataxia type 26
EEF2 SCA26
Acute myelomonocytic leukemia
FLT3 NPM1



Spinocerebellar ataxia type 26
Acute myelomonocytic leukemia

Synonym(s):
- SCA26

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C537203
External references:
No OMIM references
1 MeSH reference: D015479

No signs/symptoms info available.