All individuals with variants in gene AIFM2

1 entry on 1 page. Showing entry 1.
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     
00466508 family PubMed: Fevga 2022, Journal: Fevga 2022 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents/relatives M yes India - - - - - DYT see paper; ..., prominent segmental dystonia, proximal weakness, facial dysmorphisms; sensory neuropathy; achexia; cleft palate; hypothyroidism; left radioulnar synostosis; seizures; intellectual disability (IQ55); hypothyroidism 1 1 Johan den Dunnen
Legend   How to query  


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