All individuals with variants in gene SETD1B

17 entries on 1 page. Showing entries 1 - 17.
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00312001 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312002 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312003 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312004 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312005 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312006 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312007 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312008 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312009 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312010 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312011 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312012 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312013 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00312014 - PubMed: Faundes 2018 - - - (United Kingdom (Great Britain)) - - - - - ? - 1 1 Johan den Dunnen
00326917 8401214 PubMed: Najmabadi 2011 family, 3 affected - yes Iran - - - - - ID mild-moderate intellectual disability, coarse face, short philtrum, obesity and speech problems, coarse face, short philtrum, obesity, speech problems 1 3 Johan den Dunnen
00391754 111P - - M no Spain - - - - - ? - 1 1 Alejandro Brea-Fernández
00470281 Pat18 PubMed: Valverde de Morales 2023 3-generation family, 3 affected (son, mother, maternal grandmother M - - - - - - - NDD see paper; ..., intra-uterine growth retardation; birth 33w4d; premature birth; low birth weight (<2500g); microcephaly; motor delay; speech delay; sterotypies, easily frustrated; autism; intellectual disability, developmental delay; no seizures; no hypotonia; MRI discrete enlargement of the occipital horns associated with moderate white matter deep posterior periventricular hypersignals; sleep problems, wakes frequently; special education; no feeding difficulties/no failure to thrive; GERD; no hearing loss; myopia, astigmatism; no cleft palate/no palatal anomalies; no cardiac defect; cryptorchidism and phimosis; valgus flat feet, needs orthotics to walk; no plagiocephaly; no single palmar crease; no integumentary; normal teeth; otitits 1 3 Johan den Dunnen
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