All individuals with variants in gene NPHS1

104 entries on 2 pages. Showing entries 1 - 100.
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Data_av     

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00000004 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000007 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000008 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000009 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000012 - PubMed: Bell 2011 - - - - - - - - - autism, BMD/DMD - 1 1 Global Variome, with Curator vacancy
00000014 - PubMed: Bell 2011 - - - - - - - - - autism, BMD/DMD - 2 1 Global Variome, with Curator vacancy
00000015 - PubMed: Bell 2011 - - - - - - - - - autism, BMD/DMD - 1 1 Global Variome, with Curator vacancy
00000016 - PubMed: Bell 2011 - - - - - - - - - autism, BMD/DMD - 1 1 Global Variome, with Curator vacancy
00000017 - PubMed: Bell 2011 - - - - - - - - - autism, BMD/DMD - 1 1 Global Variome, with Curator vacancy
00000018 - PubMed: Bell 2011 - - - - - - - - - autism, BMD/DMD - 1 1 Global Variome, with Curator vacancy
00000020 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000022 - PubMed: Bell 2011 - - - - - - - - - BMD/DMD - 2 1 Global Variome, with Curator vacancy
00000024 - PubMed: Bell 2011 - - - - - - - - - BMD/DMD - 2 1 Global Variome, with Curator vacancy
00000025 - PubMed: Bell 2011 - - - - - - - - - BMD/DMD - 1 1 Global Variome, with Curator vacancy
00000026 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000027 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000028 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000031 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000037 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000039 - PubMed: Bell 2011 - - - - - - - - - ADPKD - 2 1 Global Variome, with Curator vacancy
00000041 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000042 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000043 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000046 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000047 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000048 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000051 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000052 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000054 - PubMed: Bell 2011 - - - - - - - - - ABL see paper; … 1 1 Global Variome, with Curator vacancy
00000055 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000056 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000057 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000058 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000059 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000060 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000062 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000063 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000065 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000066 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000067 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000068 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000069 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000072 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000074 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000076 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000077 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000078 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000079 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000080 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000081 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000083 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000084 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000088 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000090 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000092 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000094 - PubMed: Bell 2011 Coriell sample - - - - - - - - GA1 - 1 1 Global Variome, with Curator vacancy
00000095 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000100 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000101 - PubMed: Bell 2011 - - - - - - - - - retinal disease diffuse retinal, retinal pigment epithelium, and choroidal atrophy without evidence for choroidal neovascularization 1 1 Global Variome, with Curator vacancy
00000107 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00017906 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS1 - 2 1 Elisabet Ars Criach
00017907 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS1 - 1 1 Elisabet Ars Criach
00018452 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS congenital nephrotic syndrome, haematuria 2 1 Elisabet Ars Criach
00018845 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS - 2 1 Elisabet Ars Criach
00019409 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS - 2 1 Elisabet Ars Criach
00019411 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS - 2 1 Elisabet Ars Criach
00019413 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS - 1 1 Elisabet Ars Criach
00019917 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS1 - 1 1 Elisabet Ars Criach
00025020 - - 2-generation family, 2 affecteds, patient I.2 F yes Germany white - - - - CTRCT complete bilateral dense white autosomal recessive congenital cataract 1 1 Inst.Human Genetics - Heidelberg
00025118 - - 2-generation family, sister of PatI.2 F yes Germany white - - - - CTRCT complete bilateral dense white autosomal recessive congenital cataract 1 1 Inst.Human Genetics - Heidelberg
00025124 - - Father of 00025020 and 00025118 M ? Germany white - - - - Healthy/Control - 1 1 Inst.Human Genetics - Heidelberg
00025125 - - Mother of 00025020 and 00025118 F ? Germany white - - - - Healthy/Control - 1 1 Inst.Human Genetics - Heidelberg
00032340 - PubMed: Slavotinek 2015, Journal: Slavotinek 2015 patient, unaffected heterozygous carrier parents - ? United States - 00y07m - - - ? see paper; cerebral ventriculomegaly, echogenic kidneys with histopathological findings of congenital nephrosis, .. 1 1 Johan den Dunnen
00050595 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? nephrotic syndrome, specific learning disability, macrocephaly postnatal, hemiplegia 2 1 Johan den Dunnen
00054892 - - - - - - Hispanic - - - - glaucoma congenital glaucoma, nephrotic syndrome, developmental delay, short stature, feeding difficulties 2 1 Elena Semina
00226216 Pat1 PubMed: Aya 2000 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives - - Japan - - - - - NPHS see paper; ... 3 1 Johan den Dunnen
00292083 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00292084 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00292085 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00292086 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00292087 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 9 Mohammed Faruq
00292088 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 13 Mohammed Faruq
00292089 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 123 Mohammed Faruq
00292090 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00292091 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 17 Mohammed Faruq
00292092 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00292093 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00292094 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 19 Mohammed Faruq
00292095 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00301406 - - - ? - (Germany) - - - - - ? Prelingual sensorineural hearing impairment (HP:0000399); Thickened nuchal skin fold (HP:0000474); Delayed speech and language development (HP:0000750); Seizures (HP:0001250); Decreased antibody level in blood (HP:0004313); Relative macrocephaly (HP:0004482); Diffuse white matter abnormalities (HP:0007204); Congenital nephrotic syndrome (HP:0008677); Ureter duplex (HP:0012572) 1 1 IMGAG
00304656 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00306210 109 - - M - China - - - - - NPHS1 - 1 1 Sha Hong
00308758 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00308759 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00308760 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00308761 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00314940 NS301 PubMed: Abid 2018, Journal: Abid 2018 family history M - Pakistan - - - - - NPHS steroid resistant nephrotic syndrome; no response 1 1 Aiysha Abid
00314954 NS1401 PubMed: Abid 2018, Journal: Abid 2018 family history M - Pakistan - - - - - NPHS biopsy focal segmental glomerular sclerosis; steroid resistant nephrotic syndrome; end stage renal disease 1 1 Aiysha Abid
00380420 DRAGoN_62 - - ? - Malaysia - - - - - NPHS - 1 1 Kar-Hui Ng
00414704 NA01210 PubMed: Bell 2011 - ? - - - - - - - retinal disease - 1 1 LOVD
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