Cytoscape Web
Click node...


1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Nodular urticaria pigmentosa
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency

KIT STAT1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIT
(0.79)
STAT1



Citations in the biomedical literature:


Nodular urticaria pigmentosa
KIT
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
STAT1



Nodular urticaria pigmentosa
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- MSMD due to partial STAT1 deficiency
- MSMD due to partial signal transducer and activator of transcription 1 deficiency
- Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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

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

No signs/symptoms info available.