All individuals with variants in gene VLDLR

16 entries on 1 page. Showing entries 1 - 16.
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00050559 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected mother/child F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay 1 2 Johan den Dunnen
00057180 - - - F no Italy - - - - - CAMRQ1 At 22 months of age, the patient showed global hypotonia, truncal ataxia, nystagmus, intentional tremor, dysmetria and motor delay. At age of 12 years mild dysarthria, moderate intellectual impairment and mild ataxia gait were present, nystagmus was absent and walking without support. MRI, performed at 3 and 9 years of age, showed marked but not progressive ponto-cerebellar hypoplasia associated to mild simplification of cortical gyration 1 1 Enza Maria Valente
00210004 - - - M - Germany - - - - - - HP:0012110 (Hypoplasia of the pons); HP:0006955 (Olivopontocerebellar hypoplasia) 1 1 Andreas Laner
00210055 IP16 PubMed: Vadgama 2019, Journal: Vadgama 2019 - M - - - - - - - SCZD Has unaffected MZ twin 1 1 Nirmal Vadgama
00235444 Family A PubMed: Ozcelik 2008 3-generation family, 5 affected (2F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Turkey - - - - - ? see paper; ..., cerebellar hypoplasia, quadrupedal locomotion 1 5 Johan den Dunnen
00235445 Family D PubMed: Ozcelik 2008 3-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents/relatives F;M yes Turkey - - - - - ? see paper; ..., cerebellar hypoplasia, quadrupedal locomotion 1 3 Johan den Dunnen
00294836 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00294837 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 138 Mohammed Faruq
00305246 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00387808 M8700052 PubMed: Hu 2019 family, 3 affected individuals, third cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, no microcephaly 1 3 Johan den Dunnen
00401567 157P - - F no Spain - - - - - ID - 1 1 Alejandro Brea-Fernández
00415922 CHRO158_W07-1637 PubMed: Wissinger 2011 - F - - - - - - - retinal disease - 1 1 LOVD
00448668 FamPat1 PubMed: Holling 2024 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F yes Egypt - - - - - DD neurodevelopmental disorder without features of VLDLR cerebellar hypoplasia 1 2 Tess Holling
00448669 FamPat2 PubMed: Holling 2024 sister F - Egypt - - - - - DD neurodevelopmental disorder without features of VLDLR cerebellar hypoplasia 1 1 Tess Holling
00467635 FamPat18 PubMed: Elmas 2019 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents F yes Turkey - - - - - ? see paper; ..., neurological disorders; neuromotor developmental delay, modarete learning disability, delayed psychosocial development, macrocephaly, chronic constipation, strabismus; MRI dilated at 4th ventricles, vermis and bilateral cerebellar hemisphere hypoplasia, pachygyria; no cardiac anomalies 1 2 Johan den Dunnen
00467636 FamPat19 PubMed: Elmas 2019 brother M yes Turkey - - - - - ? see paper; ..., neurological disorders; neuromotor developmental delay, severe learning disability, delayed psychosocial development, chronic constipation, strabismus; MRI periventricular hyperintensity, vermis and bilateral cerebellar hemisphere hypoplasia, pachygyria; no cardiac anomalies 1 1 Johan den Dunnen
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