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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Charcot-Marie-Tooth disease type 2B2
Chronic myeloid leukemia

MED25 ABL1
BCR
RUNX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MED25
(0.68)
ABL1



Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 2B2
MED25
Chronic myeloid leukemia
ABL1 BCR RUNX1



Charcot-Marie-Tooth disease type 2B2
Chronic myeloid leukemia

Synonym(s):
- AR-CMT2B2
- Autosomal recessive axonal CMT4C3
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2

Synonym(s):
- Chronic granulocytic leukemia
- Chronic myelogenous leukemia

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:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
1 OMIM reference -
1 MeSH reference: C537991
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.