All individuals with variants in gene GPRC5B

3 entries on 1 page. Showing entries 1 - 3.
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     
00441736 Fam1Pat1-EL104 PubMed: Passchier 2023 - M no - - - - - - MLC normal initial cognitive development; normal initial motor development; 9m-increased OFC; never walked; 4y-start motor decline; 6y-full wheelchair dependency; 4y-start cognitive decline; rage; no history psychiatric diagnoses; 4y-refractory generalized seizures; no status epilepticus; OFC >+2SD; clumsiness; spasticity of arms; spasticity of legs; no gait/truncal ataxia; no appendicular ataxia; no dystonia; no rigidity; dysarthria; no dysphagia; severe cognitive deficit 1 1 Rogier Min
00441737 Fam2Pat2-EL919 PubMed: Passchier 2023 - M no - - - - - - MLC mildly delayed initial cognitive development; mildly delayed initial motor development; 7m-increased OFC; 3y-walk; 4y-start motor decline; 5y-loss unsupported walking; 6y-full wheelchair dependency; 15y-start cognitive decline; no behavioural problems; no history psychiatric diagnoses; 14y-occasional generalized seizures; OFC 62 cm (>+2SD); clumsiness; spasticity of arms; spasticity of legs; gait/truncal ataxia; appendicular ataxia; dystonia; dysarthria; dysphagia; mild cognitive deficit; no autistic features 1 1 Rogier Min
00441738 Fam3Pat3-EL138 PubMed: Passchier 2023 - F no - - - - - - MLC normal initial cognitive development; normal initial motor development; 6m-increased OFC; 13m-walk; 8y-start motor decline; 8y-loss unsupported walking; 12y-full wheelchair dependency; 14y-start cognitive decline; no behavioural problems; 14y-depression; two single seizures after fall (adulthood); no status epilepticus; OFC 61.5 cm (>+2SD); clumsiness; spasticity of arms; spasticity of legs; gait/truncal ataxia; appendicular ataxia; no dystonia; rigidity; dysarthria; no dysphagia; mild cognitive deficit; no autistic features 1 1 Rogier Min
Legend   How to query  


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