All individuals with variants in gene SUCLG1

5 entries on 1 page. Showing entries 1 - 5.
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     
00037217 - - - - - Germany - - - - - ? MGZ 49300: hypotonia, high lactate level, myopathology similar to spinal muscular atrophy; MGZ 57848: suspected mitochondrial myopathy; MGZ 67537: suspected Leigh syndrome; MGZ 71479: the above-mentioned patient has clinical findings indicative of Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria 1 1 Andreas Laner
00327547 family PubMed: Beck 2014 2-generation family, 5 affected (2F, 3M) F;M yes Iraq - - - - - retinal disease see paper; ..., Leber congenital amaurosis , Joubert syndrome, polycystic kidney disease 1 5 Johan den Dunnen
00391864 036P - - F no Spain - - - - - MTDPS - 2 1 Alejandro Brea-Fernández
00451440 3bINP-028 PubMed: Vela-Amieva 2024 - F no Mexico Mexican 12y04m - - - MTDPS9 Short stature, low weight, intellectual disability, developmental regression, organic aciduria 2 1 Miriam Erandi Reyna-Fabián
00451646 3bINP-084 PubMed: Vela-Amieva 2024 - F no Mexico Mexican - - - - MTDPS9 Severe intellectual disability, Developmental regression 2 1 Miriam Erandi Reyna-Fabián
Legend   How to query  


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