Disease #06823 (CONDCA (Neurodegeneration, childhood-onset, with cerebellar atrophy), OMIM:618276)

Official abbreviation CONDCA
Name Neurodegeneration, childhood-onset, with cerebellar atrophy
OMIM ID 618276
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene AGTPBP1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00433032 - - - M yes Egypt - - - - - CONDCA - - AGTPBP1 1 1 Alaaeldin Fayez
00433034 - - - M yes Egypt - - - - - CONDCA - - AGTPBP1 1 1 Alaaeldin Fayez
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