All individuals with variants in gene WDR81

11 entries on 1 page. Showing entries 1 - 11.
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00073159 - ATX478 - F - France - - - - - SCAR - 2 1 Claire Guissart
00080793 - PubMed: Trujillano 2017 no information from parents - - - - - - - - CAMRQ2 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 (OMIM:610185) 1 1 Daniel Trujillano
00080872 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - CAMRQ2 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 (OMIM:610185) 1 1 Daniel Trujillano
00225674 25558065-Fam13DG0010 PubMed: Alazami 2015, Journal: Alazami 2015 - - yes Saudi Arabia - - - - - ? see paper; …, neonatal death due to severe brain malformation (hydranencephaly and severe cerebellar hypoplasia) 1 1 Johan den Dunnen
00291644 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 183 Mohammed Faruq
00301735 17-8378 PubMed: Maddirevula 2019 - - yes Saudi Arabia - - - - - ? two children died with severe hydrocephalus, 2 healthy children 1 1 Johan den Dunnen
00304567 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00307982 17DG0783 PubMed: Anazi 2017 simplex case M - - - - - - - ID see paper; ..., Global developmental delay, Developmental regression, Microcephaly, Dandy-Walker malformation, Spasticity, Failure to thrive 1 1 Johan den Dunnen
00361545 13DG0010 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; intellectual disability and ataxia 1 1 Johan den Dunnen
00426169 10SS12400 PubMed: Al-Kasbi 2022 patient, other affecteds in family M - Oman - - - - - ID - 1 1 Johan den Dunnen
00470640 Pat1 PubMed: Horbacz 2025 patient, affected maternal uncle M - Poland - - - - - scoliosis see paper; ... scoliosis, no other skeletal defects; back pain; 1 1 Johan den Dunnen
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