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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute myeloblastic leukemia with maturation
Spinocerebellar ataxia type 36

FLT3 NOP56
KIT
NPM1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NPM1
(0.63)
NOP56



Citations in the biomedical literature:


Acute myeloblastic leukemia with maturation
FLT3 KIT NPM1
Spinocerebellar ataxia type 36
NOP56



Acute myeloblastic leukemia with maturation
Spinocerebellar ataxia type 36

Synonym(s):
- Acute myeloblastic leukemia type 2

Synonym(s):
- SCA36

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.