Phenotypes for disease #00142 (SCA5 (ataxia, spinocerebellar, type 5 (SCA-5)), OMIM:600224)

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000000655 - Familial, autosomal recessive - - - - - - - Hanno Bolz 00001238
0000041535 cerebellar ataxia Unknown - OPA - - - ataxia, neuropathy, cataract - Erik-Jan Kamsteeg 00054871
0000115945 - Isolated (sporadic) 01y06m - - - - cerebellar atrophy, Cerebellar ataxia, Moderate global developmental delay, EEG abnormality, Dolichocephaly, Convergent strabismus, Infantile muscular hypotonia, Hyporeflexia of lower limbs - Enza Maria Valente 00143194
0000127668 - Isolated (sporadic) - - 01y11m - Cerebellar atrophy, cerebellar ataxia, developmental delay, strabismus, dolicocephaly - - Enza Maria Valente 00154933
0000257682 - Unknown - - - 11y - (+) Seizure,(+) Ataxia,(+) Spastic tetraparesis,(+) Dysmetria,(+) EEG abnormality,(+) Spastic dysarthria,(+) Intellectual disability, progressive,(+) Abnormal visual electrophysiology - Andreas Laner 00362271
0000290569 50y Unknown 62y - - - - Ataxia, Abnormality of coordination, Gait ataxia, Impaired distal vibration sensation, Hyperreflexia, Cerebellar atrophy, Progressive cerebellar ataxia - Andreas Laner 00397435
0000297566 SCA Familial, autosomal dominant 33y - - 16y - 27-y male The patient presents with abnormality of movement, ataxia, fasciculations, muscle weakness, muscular hypotonia, peripheral neuropathy, skeletal muscle atrophy and tremor. - Sherifa Ahmed Hamed 00405008
0000325327 SCA Isolated (sporadic) 32 - - - - - - Sherifa Ahmed Hamed 00435089
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