Disease #04669 (SCAR20 (ataxia, spinocerebellar, autosomal recessive, type 20 (SCAR-20)), OMIM:616354)

Official abbreviation SCAR20
Name ataxia, spinocerebellar, autosomal recessive, type 20 (SCAR-20)
OMIM ID 616354
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene SNX14
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Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00080817 - PubMed: Trujillano 2017 unaffected parents - - - - - 0 - - SCAR20 Spinocerebellar ataxia type 20 (OMIM:616354) SNX14 SNX14 1 1 Daniel Trujillano
00080946 - PubMed: Trujillano 2017 unaffected parents - - - - - 0 - - SCAR20 Spinocerebellar ataxia, autosomal recessive 20 (OMIM:616354) SNX14 SNX14 1 1 Daniel Trujillano
00081088 - PubMed: Trujillano 2017 unaffected parents - - - - - 0 - - SCAR20 Spinocerebellar ataxia, autosomal recessive 20 (OMIM:616354) SNX14 SNX14 1 1 Daniel Trujillano
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