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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 associated genes
No signs/symptoms info
Spinocerebellar ataxia type 36
Idiopathic pulmonary arterial hypertension

NOP56 BMPR2
CBLN2
KCNK3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NOP56
(0.52)
BMPR2



Citations in the biomedical literature:


Spinocerebellar ataxia type 36
NOP56
Idiopathic pulmonary arterial hypertension
BMPR2 CBLN2 KCNK3



Spinocerebellar ataxia type 36
Idiopathic pulmonary arterial hypertension

Synonym(s):
- SCA36

Synonym(s):
- IPAH

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the circulatory 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:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: adult
Type of inheritance: sporadic

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

No signs/symptoms info available.