Disease #00721 (CAMRQ2 (ataxia, cerebellar, mental retardation, and dysequilibrium syndrome, type 2 (CAMRQ-2)), OMIM:610185)

Official abbreviation CAMRQ2
Name ataxia, cerebellar, mental retardation, and dysequilibrium syndrome, type 2 (CAMRQ-2)
OMIM ID 610185
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene WDR81
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00080793 - PubMed: Trujillano 2017 no information from parents - - - - - - - - CAMRQ2 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 (OMIM:610185) WDR81 WDR81 1 1 Daniel Trujillano
00080872 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - CAMRQ2 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 (OMIM:610185) WDR81 WDR81 1 1 Daniel Trujillano
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