All individuals with variants in gene PRPH

8 entries on 1 page. Showing entries 1 - 8.
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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     
00108467 28722276-FamPatIII3 PubMed: Hendee 2017, Journal: Hendee 2017 3-generation family, 10 affecteds (6F, 4M), PatIII3 M - United States white - - - - ? Congenital glaucoma Axenfeld-Rieger anomaly myopia sensorineural hearing loss congenital hypothyroidism arterial tortuosity microcephaly delayed eruption of permanent teeth femoral retroversion 1 1 Elena Semina
00290730 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 145 Mohammed Faruq
00290731 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 119 Mohammed Faruq
00290732 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 121 Mohammed Faruq
00290733 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304363 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304364 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304365 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
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