Disease #05428 (atrophy, cerebellar (atrophy, cerebellar))

Official abbreviation atrophy, cerebellar
Name atrophy, cerebellar
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2018-05-11 14:19:31 +02:00 (CEST)
Date last edited N/A


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00164232 29727687-Pat1 PubMed: Burns 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents F - El Salvador - - - - - atrophy, cerebellar see paper; ..., cerebellar atrophy, spinal motor neuronopathy EXOSC9 EXOSC9 1 1 Johan den Dunnen
00164233 29727687-Pat2 PubMed: Burns 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Canada;Jamaica African-Canadian;Jamaican 01y03m - - - atrophy, cerebellar see paper; ..., cerebellar atrophy, spinal motor neuronopathy EXOSC9 EXOSC9 2 1 Johan den Dunnen
00164234 29727687-Pat3 PubMed: Burns 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents F yes Saudi Arabia - - - - - atrophy, cerebellar see paper; ..., cerebellar atrophy, spinal motor neuronopathy EXOSC9 EXOSC9 1 1 Johan den Dunnen
00164235 29727687-Pat4 PubMed: Burns 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents F - - African-European-Fillipino - - - - atrophy, cerebellar see paper; ..., cerebellar atrophy, spinal motor neuronopathy EXOSC9 EXOSC9 1 1 Johan den Dunnen
00206903 23224214-Fam PubMed: Poulton 2013 8-generation family, 3 affected (3M), unaffected heterozygous carrier parents/relatives M yes Netherlands - - - - - atrophy, cerebellar see paper; ... PNKP PNKP 1 3 Johan den Dunnen
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