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Cerebellar ataxia-deafness-narcolepsy syndrome
1 OMIM reference -
1 associated gene
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
Cerebellar ataxia-deafness-narcolepsy syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

DNMT1
(UniProt - OMIM)
 ARHGDIA
(UniProt - OMIM)
PLCE1
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)
WT1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DNMT1
(0.63)
WT1


Citations in the biomedical literature:


Cerebellar ataxia-deafness-narcolepsy syndrome
DNMT1
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
ARHGDIA PLCE1 PTPRO WT1



Cerebellar ataxia-deafness-narcolepsy syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

Synonym(s):
- ADCA-DN
- Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
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.