All individuals with variants in gene WDR73

11 entries on 1 page. Showing entries 1 - 11.
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00039413 - WDR73 - F yes Austria Austria - - - - ? - 1 1 Andreas Janecke
00039414 - WDR73 - M yes Lebanon Lebanon - - - - GAMOS1 - 1 5 Andreas Janecke
00039415 - WDR73 - F yes India India - - - - ? - 1 1 Andreas Janecke
00039416 - WDR73 - F yes Turkey Turkey - - - - ? - 1 1 Andreas Janecke
00039417 - WDR73 - F yes Somalia Somalia - - - - ? - 1 1 Andreas Janecke
00043751 - PubMed: Colin 2014, Journal: Colin 2014 2-generation family, 2 affected males, unaffected heterozygous carrier parents M no Morocco - - - - - GAMOS1 see paper; secondary microcephaly, severe neurological impairment, nephrotic syndrome (one), peripheral hypertonia, axial hypotonia (at 4m), nystagmus (one), epileptic spasms, ID; brain MRI cerebellar atrophy, thin corpus callosum (one), subtentorial atrophy (one); facial dysmorphy, optic atrophy, ... 1 2 Johan den Dunnen
00043752 - PubMed: Colin 2014, Journal: Colin 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents/brother M yes Turkey Turkish - - - - GAMOS1 see paper; focal segmental glomerulosclerosis, podocyte hypertrophy, no end-stage kidney disease; head circumference (5m -2 SD, 10y -3 SDs), hypertonia, ID, spasticity, cerebellar atrophy, thin corpus callosum, subtentorial atrophy, ventricular dilation, facial dysmorphy, abnormal visual evoked potentials, optic atrophy, ... 1 1 Johan den Dunnen
00183062 23033978-Trio59 PubMed: de Ligt 2012 - F - Netherlands - - - - - ID see paper; … 1 1 Johan den Dunnen
00318009 PKMR242 PubMed: Riazuddin 2017 - - yes Pakistan - - - - - ID Mild to moderate ID, microcephaly, Dental anomalies, Weak limbs, defects in all affected, Besides these featuresIV:3 has defects in vertebral column and disordered walk. In addition to above features IV:4 has weak limbs 1 1 Johan den Dunnen
00399294 166720 - - F yes Syria - - - - - GAMOS1 Global developmental delay, Profound global developmental delay, Short stature, Microcephaly, Spasticity, Nystagmus, Horizontal pendular nystagmus, Cerebellar atrophy, Abnormality of the basal ganglia, Abnormality of extrapyramidal motor function 1 1 Andreas Laner
00415258 13 PubMed: Alfares 2018 - F - - - - - - - retinal disease OMIM: 251300; developmental delay, delayed myelination of the white matter, and poor vision 1 1 LOVD
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