All individuals with variants in gene LBR

17 entries on 1 page. Showing entries 1 - 17.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00240204 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 27 LOVD
00240205 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 200 LOVD
00240206 - - - - - - - - - - - Healthy/Control - 7 1 LOVD
00240207 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 1 LOVD
00240208 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 142 LOVD
00240209 - - - - - France - - - - - ? scleroderma 1 1 LOVD
00240210 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 37 LOVD
00240211 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 184 LOVD
00240212 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 24 LOVD
00240213 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 204 LOVD
00240214 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 213 LOVD
00240215 - - patients (scleroderma) and controls - - France - - - - - Healthy/Control - 1 7 LOVD
00240216 - - - - - France - - - - - ? scleroderma 1 1 LOVD
00289741 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00331498 15DG1157 PubMed: Maddirevula 2018 isolated case M yes - - - - - - skeletal dysplasia Non-Arab ( Skeletal dysplasia, Depressed nasal bridge, Retrognathia 1 1 LOVD
00388440 R09-162A PubMed: Zhang-2019 - - - - Latino - - - - ? - 2 1 LOVD
00434444 256215 - prenatal trio exom after ultrasound abnormalities ? likely - - - - - - GRBGD Abnormality of prenatal development or birth, Skeletal dysplasia, Thickened nuchal skin fold, Micromelia, Postaxial polydactyly, Abnormal thorax morphology, Single umbilical artery 1 1 Andreas Laner
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