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Autosomal recessive spastic paraplegia type 18
1 OMIM reference -
1 associated gene
22 connected diseases
No signs/symptoms info
Disease Type of connection
Juvenile primary lateral sclerosis
Recessive intellectual disability - motor dysfunction - multiple joint contractures
Spinocerebellar ataxia type 15 / 16
Spinocerebellar ataxia type 29
Fibronectin glomerulopathy
22q11.2 deletion syndrome
Autosomal agammaglobulinemia
Behavioral variant of frontotemporal dementia
CLN3 disease
Congenital bilateral absence of vas deferens
Cystic fibrosis
Early-onset autosomal dominant Alzheimer disease
Familial isolated dilated cardiomyopathy
Familial renal cell carcinoma
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Precursor B-cell acute lymphoblastic leukemia
Progressive non-fluent aphasia
Semantic dementia
T-B+ severe combined immunodeficiency due to CD3delta / CD3epsilon / CD3zeta
Spinocerebellar ataxia type 26
- SPG18

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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
ERLIN2 O94905611605
No signs/symptoms info available.