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Spinocerebellar ataxia type 36
1 OMIM reference -
1 associated gene
37 connected diseases
No signs/symptoms info
Disease Type of connection
Blackfan-Diamond anemia
Amyotrophic lateral sclerosis
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Estrogen resistance syndrome
Treacher-Collins syndrome
46,XY partial gonadal dysgenesis
ANE syndrome
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Autoimmune polyendocrinopathy type 1
Autosomal dominant macrothrombocytopenia
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Combined oxidative phosphorylation defect type 4
Familial thoracic aortic aneurysm and aortic dissection
Familial visceral myopathy
Frontotemporal dementia with motor neuron disease
Hypotrichosis simplex
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Lissencephaly due to TUBA1A mutation
Moyamoya disease
Pseudohypoaldosteronism type 2E
Spinocerebellar ataxia type 26
Wolf-Hirschhorn syndrome
Hereditary breast and ovarian cancer syndrome
Nijmegen breakage syndrome-like disorder
Heritable pulmonary arterial hypertension
Idiopathic pulmonary arterial hypertension
Pulmonary venoocclusive disease
Anauxetic dysplasia
Generalized congenital lipodystrophy with myopathy
Synonym(s):
- SCA36
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
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
Gene symbol UniProt reference OMIM reference
NOP56 O00567614154
No signs/symptoms info available.