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Spinocerebellar ataxia type 26
1 OMIM reference -
2 associated genes
58 connected diseases
No signs/symptoms info
Disease Type of connection
Blackfan-Diamond anemia
Familial pancreatic carcinoma
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Charcot-Marie-Tooth disease type 4D
Fibronectin glomerulopathy
Familial melanoma
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Amyotrophic lateral sclerosis
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Cabezas syndrome
Constitutional mismatch repair deficiency syndrome
Craniometaphyseal dysplasia
Dedifferentiated liposarcoma
Estrogen resistance syndrome
Frontotemporal dementia with motor neuron disease
Glycogen storage disease due to liver phosphorylase kinase deficiency
Hemolytic anemia due to glutathione reductase deficiency
Hereditary nonpolyposis colon cancer
Hypoplastic left heart syndrome
Lethal polymalformative syndrome, Boissel type
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Mitochondrial neurogastrointestinal encephalomyopathy
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Oculodentodigital dysplasia
Pseudohypoaldosteronism type 2E
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Severe combined immunodeficiency due to DNA-PKcs deficiency
Spinocerebellar ataxia type 36
Split hand-split foot malformation
Syndactyly type 3
Well-differentiated liposarcoma
Williams syndrome
Young adult-onset Parkinsonism
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Autosomal recessive spastic paraplegia type 18
Familial infantile bilateral striatal necrosis
Hereditary pheochromocytoma-paraganglioma
Hypotrichosis simplex
Juvenile primary lateral sclerosis
Posterior polar cataract
Recessive intellectual disability - motor dysfunction - multiple joint contractures
Total congenital cataract
- SCA26

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

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

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C537203

Gene symbol UniProt reference OMIM reference
EEF2 P13639130610
No signs/symptoms info available.