All individuals with variants in gene BCKDK

7 entries on 1 page. Showing entries 1 - 7.
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     
00004118 - - - - no Spain - - - - - autism - 1 1 Alfonso Luis Oyarzábal Sanz
00004119 - - - - - Afghanistan - - - - - autism - 1 1 Alfonso Luis Oyarzábal Sanz
00050683 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) M - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, abnormality of the outer ear, prominent metopic ridge, narrow mouth, inferior vermis hypoplasia, delayed speech and language development 1 2 Johan den Dunnen
00275672 FamMCP102Pat3 PubMed: Santos-Cortez 2018 4-generation family, 2 affected (F, M), unaffected heterozygous carrier parents/relatives M yes Pakistan - - - - - ID OFC 45.5cm; IQ 50, moderate intellectual disability (HP:0002342); microcephaly, poor speech, hyperactive behavior, unbalanced movement 1 2 Johan den Dunnen
00275673 FamMCP102Pat4 PubMed: Santos-Cortez 2018 - F yes Pakistan - - - - - ID OFC 43cm; IQ 45, moderate intellectual disability (HP:0002342) 1 1 Johan den Dunnen
00390025 3 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Pale and tilted optic disk associated to hypoplasia, tortuous retinal vessels, non-homogeneous macula 1 1 LOVD
00453031 Fam8 Journal: Paracha 2024 4-generation family, 4 affected (3F, M), heterozygous carrier parents/relatives F;M yes Pakistan - - - - - NDD severe phenotype, intellectual disability, microcephaly, behavioral abnormalities 1 4 Muhammad Umair
Legend   How to query  


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