All individuals with variants in gene NHLRC2

4 entries on 1 page. Showing entries 1 - 4.
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AscendingIndividual ID     

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00039400 Pat1;Pat13 PubMed: Bosch 2014, Journal: Bosch 2014, PubMed: Bosch 2016, Journal: Bosch 2016 - M no Netherlands - >12y - - - BBSOAS, CVI, ID Protruding ear (HP:0000411); Abnormality of the nares (HP:0005288); Thick nasal alae (HP:0009928); Abnormality of the thorax (HP:0000765); Long fingers (HP:0100807); Long toe (HP:0010511); Reduced visual acuity (HP:0007663); Nystagmus (HP:0000639); Optic atrophy (HP:0000648); Abnormal macular morphology (HP:0001103); Abnormal timing of flash visual evoked potentials (HP:0030461); Abnormal timing of pattern onset/offset visual evoked potentials (HP:0030458); Eccentric visual fixation (HP:0025549); Intellectual disability, moderate (HP:0002342); Cerebral visual impairment (HP:0100704); Neurodevelopmental delay (HP:0012758); Visual field defect (HP:0001123); Strabismus (HP:0000486) 2 1 Danielle Bosch
00300169 - - - ? - - - - - - - ? Global developmental delay (HP:0001263); Failure to thrive (HP:0001508); Cerebral atrophy (HP:0002059); Hypoplasia of the corpus callosum (HP:0002079); Chronic lung disease (HP:0006528); Abnormal ascending aorta morphology (HP:0031784) 1 1 IMGAG
00387782 M8600128 PubMed: Hu 2019 family, 2 affected individuals, third cousin parents - yes - Kurd - - - - ID syndromic intellectual disability, microcephaly (SD-3.0), epilepsy 1 2 Johan den Dunnen
00398392 - PubMed: Dan 2020 uncle of III:2 M ? China - - - - - retinal disease Nyctalopia, vision decline, vision field defect 1 1 LOVD
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