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Distal 17p13.3 microdeletion syndrome
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Chronic myeloid leukemia
1 OMIM reference -
3 associated genes
No signs/symptoms info
Distal 17p13.3 microdeletion syndrome
Chronic myeloid leukemia

YWHAE
(UniProt - OMIM)
 ABL1
(UniProt - OMIM)
BCR
(UniProt - OMIM)
RUNX1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
YWHAE
YWHAE
(0.83)
(0.52)
ABL1
BCR


Citations in the biomedical literature:


Distal 17p13.3 microdeletion syndrome
YWHAE
Chronic myeloid leukemia
ABL1 BCR RUNX1



Distal 17p13.3 microdeletion syndrome
Chronic myeloid leukemia

Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3
Synonym(s):
- Chronic granulocytic leukemia
- Chronic myelogenous leukemia
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.