Cytoscape Web
Click node...


1 associated gene
No signs/symptoms info
COMMON GENES: 1
5 associated genes
No signs/symptoms info
Typical urticaria pigmentosa
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

KIT CEBPA
FLT3
KIT
RUNX1
RUNX1T1


COMMON
GENES
KIT



Citations in the biomedical literature:


Typical urticaria pigmentosa
KIT
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
CEBPA FLT3 RUNX1 RUNX1T1



Typical urticaria pigmentosa
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

Classification (Orphanet):
- Rare allergic disease
- Rare hematologic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

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

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.