All individuals with variants in gene TBCD

11 entries on 1 page. Showing entries 1 - 11.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00143186 - - - M yes (India) Asian - - - - ? microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900) 1 1 -
00143188 - - - M yes (India) Asian - - - - ? microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900) 1 1 Joshi Stephen
00163916 P1 - - F ? Faroe Islands Faroese 01y08m - No No PEBAT - 1 1 Elsebet Østergaard
00164375 P2 - - ? - Argentina - 04y08m - - - PEBAT - 1 1 Elsebet Østergaard
00164376 P3 - - M - Faroe Islands - 02y03m - - - PEBAT - 1 6 Elsebet Østergaard
00164436 P4 - - - - Faroe Islands - 01y10m - - - PEBAT - 1 1 Elsebet Østergaard
00164437 P5 - - - - Faroe Islands - 03y09m - - - PEBAT - 1 1 Elsebet Østergaard
00164438 P6 - - - - - - 00y10m - - - PEBAT - 1 1 Elsebet Østergaard
00164439 P7 - - - - Faroe Islands - - - - - PEBAT - 1 1 Elsebet Østergaard
00164440 P8 - - - - - - 03y02m - - - PEBAT - 1 1 Elsebet Østergaard
00379729 - - two affected siblings to consanguineous parents. M yes Saudi Arabia Arabs - - - - PEBAT Both siblings have lower extremities weakness (proximal to distal) with distal muscle wasting and foot equinovarus deformities. The younger sibling has focal epilepsy. Bith have thin corpus callosum on brain MRI and their NCS/EMG is in keeping with the neuronopathic process 1 2 Nahla Alshaikh
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.