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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
10 signs/symptoms
Spinocerebellar ataxia with axonal neuropathy type 2
Apolipoprotein A-I deficiency

PIK3R5 ABCA1
SETX APOA1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SETX
(0.72)
APOA1



Citations in the biomedical literature:


Spinocerebellar ataxia with axonal neuropathy type 2
PIK3R5 SETX
Apolipoprotein A-I deficiency
ABCA1 APOA1



Spinocerebellar ataxia with axonal neuropathy type 2
Apolipoprotein A-I deficiency

Synonym(s):
- AOA2
- Ataxia - oculomotor apraxia type 2
- SCAN 2
- SCAR1

Synonym(s):
- ApoA-I deficiency
- Familial apoA-I deficiency
- Familial hypoalphalipoproteinemia

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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

External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D052456

Apolipoprotein A-I deficiency

Frequent
- Abnormal EMG / electromyogram / electropmyography
- Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase
- Anaemia
- Autosomal recessive inheritance
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Hepatitis / icterus / cholestasis
- Hyperlipidemia / hypercholesterolemia / hypertriglyceridemia
- Lymphadenopathy / polyadenopathies
- Splenomegaly
- Storage liver disease



Spinocerebellar ataxia with axonal neuropathy type 2

(no data available)