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1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
2 associated genes
No signs/symptoms info
Chronic myeloid leukemia
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

ABL1 MUC1
BCR UMOD
RUNX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ABL1
(0.79)
MUC1



Citations in the biomedical literature:


Chronic myeloid leukemia
ABL1 BCR RUNX1
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD



Chronic myeloid leukemia
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

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

Synonym(s):
- Autosomal dominant nephronophthisis

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.