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1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Proximal spinal muscular atrophy type 3
Spinocerebellar ataxia type 36

NAIP NOP56
SMN1
SMN2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SMN1
SMN2
(0.72)
(0.72)
NOP56
NOP56



Citations in the biomedical literature:


Proximal spinal muscular atrophy type 3
NAIP SMN1 SMN2
Spinocerebellar ataxia type 36
NOP56



Proximal spinal muscular atrophy type 3
Spinocerebellar ataxia type 36

Synonym(s):
- Juvenile spinal muscular atrophy
- Kugelberg-Welander disease
- SMA type 3
- SMA-III
- SMA3

Synonym(s):
- SCA36

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.