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Oculootodental syndrome
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
4 OMIM references -
4 associated genes
No signs/symptoms info
Oculootodental syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

FADD
(UniProt - OMIM)
 ARHGDIA
(UniProt - OMIM)
FGF3
(UniProt - OMIM)
 PLCE1
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)
WT1
(UniProt - OMIM)

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


Citations in the biomedical literature:


Oculootodental syndrome
FADD FGF3
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
ARHGDIA PLCE1 PTPRO WT1



Oculootodental syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

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