All individuals with variants in gene PHYH

15 entries on 1 page. Showing entries 1 - 15.
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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     
00104991 64ORG1 PubMed: de Castro-Miró 2016 - M no Argentina - - - - - Refsum - 2 1 Marta de Castro-Miró
00155523 - Sharon, submitted - M yes Israel Arab-Muslim - - - - Refsum - 1 1 Dror Sharon
00290002 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00309299 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00328233 G008151 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 2 1 LOVD
00333352 Pat5 PubMed: Costa 2017 - M - Brazil - - - - - retinal disease see paper; ... 1 1 LOVD
00358964 Case72007 PubMed: Tiwari 2016 see paper M - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00358969 Case71133 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00373848 Rp58 PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - retinal disease see paper; ... 1 1 LOVD
00374437 S-340 PubMed: Ganapathy 2019 - - - India - - - - - ? Frequent falls, abnormal gait, muscle weakness, attention deficit, round face, short neck and ichthyosis 1 1 Johan den Dunnen
00389363 647 PubMed: Weisschuh 2020 Filing key number: 233, unclassified / mixed, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 2 1 LOVD
00389364 648 PubMed: Weisschuh 2020 Filing key number: 233, unclassified / mixed, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 2 1 LOVD
00390343 G008151 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - retinal disease - 2 1 LOVD
00426926 30_35 PubMed: Zhu 2022 family 30, individual 35 M - - - - - - - retinal disease - 1 1 LOVD
00447207 MISC-303 PubMed: Weisschuh 2024 family, 2 affected M - Germany - - - - - ? - 1 2 Johan den Dunnen
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