All individuals with variants in gene ADAT3

12 entries on 1 page. Showing entries 1 - 12.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00080884 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MRT36 Mental retardation, autosomal recessive 36 (OMIM:615286) 1 1 Daniel Trujillano
00080980 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MRT36 Mental retardation, autosomal recessive 36 (OMIM:615286) 1 1 Daniel Trujillano
00081076 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MRT36 Mental retardation, autosomal recessive 36 (OMIM:615286) 1 1 Daniel Trujillano
00361520 11DG0313 PubMed: Anazi 2017 familial M yes Saudi Arabia - - - - - ID not syndromic; intellectual disability and strabismus 1 1 Johan den Dunnen
00361566 12DG0628 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; intellectual disability, seizures 1 1 Johan den Dunnen
00361574 10DG1658 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; intellectual disability, short stature, strabismus, seizurs, brain atrophy 1 1 Johan den Dunnen
00361594 08F-00103 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; intellectual disability with strabismus 1 1 Johan den Dunnen
00361622 10DG0053 PubMed: Anazi 2017 familial M yes Saudi Arabia - - - - - ID not syndromic; intellectual disability with strabismus 1 1 Johan den Dunnen
00361623 11DG1198 PubMed: Anazi 2017 familial M yes Saudi Arabia - - - - - ID not syndromic; intellectual disability, microcephaly, strabismus, ADHD 1 1 Johan den Dunnen
00361627 09DG00479 PubMed: Anazi 2017 familial M yes Saudi Arabia - - - - - ID not syndromic; intellectual disability with strabismus 1 1 Johan den Dunnen
00415247 2 PubMed: Alfares 2018 - M - - - - - - - retinal disease OMIM: 602014; failure to thrive, developmental and speech delay, and celiac disease 1 1 LOVD
00415248 3 PubMed: Alfares 2018 - M - - - - - - - retinal disease OMIM: 615286; muscular hypotonia, strabismus, brachycephalic triangle long face, pointed chin, long philtrum, thin upper lips, and epicanthal folds with squint and rocker bottom feet 1 1 LOVD
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