All individuals with variants in gene ETHE1

13 entries on 1 page. Showing entries 1 - 13.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00035712 - - - - - Germany - - - - - ? Brother: Ethylmalonacid-enzephalopathy 1 1 Andreas Laner
00035713 - - - - - Germany - - - - - ? Brother: Ethylmalonacid-enzephalopathy 1 1 Andreas Laner
00035714 - - - - - Germany - - - - - ? suspected familiar ataxia type II 1 1 Andreas Laner
00035715 - - - - - Germany - - - - - ? Brother: Ethylmalonacid-enzephalopathy 1 1 Andreas Laner
00035716 - - - - - Germany - - - - - ? Ethylmalonacid-enzephalopathy 1 1 Andreas Laner
00035717 - - - - - Germany - - - - - ? Ethylmalonacid-enzephalopathy 1 1 Andreas Laner
00080947 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - EE Ethylmalonic encephalopathy (OMIM:602473) 1 1 Daniel Trujillano
00292145 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 5 Mohammed Faruq
00292146 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00292147 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00296595 Pat28 PubMed: Kemp 2011, PubMed: Taylor 2014 2 affected M - Turkey - - - - - ? muscle affected; central nervous system affected; heart not affected; liver not affected; lactic acidosis 1 2 Johan den Dunnen
00466856 NDAR03-1 - 2 affected (2M), unaffected carrier parents M yes Pakistan South asian - - - - EE intellectual disability (HP:0010864), Muscular hypotonia (HP:0001252), facial dysmorphism (HP:0001999), and , delayed global milestones(HP:0001263), aggression 1 2 Arisha Rasheed
00466857 NDAR03-2 - sib M yes Pakistan Asia-S - - - - EE Intellectual disability (HP:0010864), Muscular hypotonia (HP:0001252), facial dysmorphism (HP:0001999), and , delayed global milestones(HP:0001263), seizures 1 1 Arisha Rasheed
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