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Oculootodental syndrome
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
1 associated gene
No signs/symptoms info
Oculootodental syndrome
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency

FADD
(UniProt - OMIM)
 STAT1
(UniProt - OMIM)
FGF3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FADD
(0.55)
STAT1


Citations in the biomedical literature:


Oculootodental syndrome
FADD FGF3
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
STAT1



Oculootodental syndrome
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency

Synonym(s):
- OOD
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 developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the digestive system -
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:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.