Cytoscape Web
Click node...

Telangiectasia macularis eruptiva perstans
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
1 associated gene
No signs/symptoms info
Telangiectasia macularis eruptiva perstans
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency

KIT
(UniProt - OMIM)
 STAT1
(UniProt - OMIM)

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


Citations in the biomedical literature:


Telangiectasia macularis eruptiva perstans
KIT
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
STAT1



Telangiectasia macularis eruptiva perstans
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):
- Congenital malformations, deformations and chromosomal abnormalities -
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.