All individuals with variants in gene SLC12A3

157 entries on 2 pages. Showing entries 1 - 100.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 1 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00080875 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - GTLMNS Gitelman syndrome (OMIM:263800) 1 1 Daniel Trujillano
00107880 FamJorPatIII1 PubMed: Bonnard 2012 2-generation family, 3 affected sibs, unaffected heterozygous carrier parents/relatives (F, 2M) M yes Jordan - - - - - HMMS craniosynostosis; brachycephaly; bulging midface; laterally sparse eyebrows; severe telecanthus/hypertelorism; severe progressive myopia; absence/dysfunction of nasolacrimal structures; no dysfunction of parotid glands; broad nasal bridge/pointed nasal tips/anteverted nostrils; high arched palate; smooth/long philtrum; thin upper vermillion border/wide mouth; loss of lamina dura; thin enamel/enamel hypoplasia; low-set/ear abnormalities; no bilateral preauricular tags; sensori neural hearing impairment; mild micrognathia; low posterior hair line/extra frontal hair whorl; generalized osteopenia; long bone fractures; hip dysplasia; no pectus excavatum; pterygium colli/slopping shoulder; no syndactyly/tapering fingers/long toes/5th finger clinodactyly; thumb deviation/ectopic finger creases/long fingers/short index; tiny patent ductus arteriosus; no mild mitral regurgitation; no atrial septal defect; intraventricular conduction delay; no total A-V canal; inguinal hernia; no hypoparathyroidism; cryptorchidism and absence of gonad activity; microcytic hypochromic anemia; moderate psychomotor retardation; unclear speech 1 3 Johan den Dunnen
00269921 - - - M - - - - - - - ? Abnormality of acetylcarnitine metabolism (HP:0012071); Periodic paralysis (HP:0003768); Rhabdomyolysis (HP:0003201); Exercise-induced myalgia (HP:0003738) 2 1 Andreas Laner
00291494 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 34 Mohammed Faruq
00291495 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291496 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 72 Mohammed Faruq
00291497 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00304520 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00308006 - - - F - - - - - - - ? Hypokalemia (HP:0002900) 2 1 Andreas Laner
00320250 PT274 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320251 PT435 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320252 PT470 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320253 PT491 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320254 PT552 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320255 PT620 - - - - Japan Asian - - - - GTLMNS - 3 1 Takayasu Mori
00320271 PT635 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320272 PT641 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320273 PT662 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320274 PT664 - - - - Japan Asian - - - - GTLMNS - 3 1 Takayasu Mori
00320275 PT665 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320276 PT694 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320277 PT861 - - - - Japan Asian - - - - GTLMNS - 3 1 Takayasu Mori
00320278 PT901 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320279 PT928 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320280 PT934 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320281 PT936 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320282 PT937 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320283 PT944 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320311 PT948 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320312 PT1043 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320313 PT1075 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320314 PT1092 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320315 PT1111 - - - - Japan Asian - - - - GTLMNS - 3 1 Takayasu Mori
00320316 PT1116 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320317 PT1152 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320318 PT1159 - - - - Japan Asian - - - - GTLMNS - 2 1 Takayasu Mori
00320319 PT547 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00320320 PT1031 - - - - Japan Asian - - - - GTLMNS - 1 1 Takayasu Mori
00331603 175691 - - M ? Germany - - - - - GTLMNS severe hypokalemia, clinical Gitelmann-syndrome 2 1 Andreas Laner
00362002 Pat5AB PubMed: Duvvari 2016 patient - - Netherlands white - - - - retinal disease - 1 1 LOVD
00362011 Fam3 PubMed: Duvvari 2016 2-generation family, 4 affected (3F, M) - - Netherlands white - - - - retinal disease - 1 3 LOVD
00373352 179285 - - M ? Turkey - - - - - GTLMNS clinically Gitelmann syndrome, cardiac arrhythmia, SA block 2 1 Andreas Laner
00395054 K17 PubMed: Zacchia 2021 - F - (Italy) - - - - - retinal disease - 1 1 LOVD
00395055 K18 PubMed: Zacchia 2021 - - - (Italy) - - - - - retinal disease - 2 1 LOVD
00395056 K19 PubMed: Zacchia 2021 - F - (Italy) - - - - - retinal disease - 2 1 LOVD
00395057 K39 PubMed: Zacchia 2021 - F - (Italy) - - - - - retinal disease - 2 1 LOVD
00395059 K106 PubMed: Zacchia 2021 - ? - (Italy) - - - - - retinal disease - 1 1 LOVD
00414364 WHP31 PubMed: Sun 2018 - M - China - - - - - ? - 2 1 LOVD
00414410 WHP77 PubMed: Sun 2018 - M - China - - - - - ? - 1 1 LOVD
00414458 WHP125 PubMed: Sun 2018 - M - China - - - - - ? - 2 1 LOVD
00437029 Pat86 PubMed: Viering 2023, Journal: Viering 2023 - F - France - - - - - GTLMNS hypokalemia 2 1 Johan den Dunnen
00437030 Pat106 PubMed: Viering 2023, Journal: Viering 2023 - M - Germany - - - - - GTLMNS incidental finding 2 1 Johan den Dunnen
00437031 Pat15 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M no France - - - - - GTLMNS hypokalemia; hypomagnesemia; hypocalciuria; 2 1 Johan den Dunnen
00437032 Pat12 PubMed: Viering 2023, Journal: Viering 2023 - M - France - - - - - GTLMNS hypokalemia; chronic hyperaldosteronism; episode of gastroenteritis 2 1 Johan den Dunnen
00437033 Pat32 PubMed: Viering 2023, Journal: Viering 2023 - F - France - - - - - GTLMNS hypokalemia; hypomagnesemia; hypocalciuria 2 1 Johan den Dunnen
00437034 Pat59 PubMed: Viering 2023, Journal: Viering 2023 - F - France - - - - - GTLMNS hypokalemia; hypomagnesemia; metabolic alkalosis; asthenia 2 1 Johan den Dunnen
00437035 Pat104 PubMed: Viering 2023, Journal: Viering 2023 - M - Germany - - - - - GTLMNS - 2 1 Johan den Dunnen
00437036 Pat112 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, 1 affected, unaffected parents M - Germany - - - - - GTLMNS - 2 1 Johan den Dunnen
00437037 Pat3 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and 2 affected sisters, unaffected parents M no France - - - - - GTLMNS hypokalemia; cramps; hypochloremia; hand and leg myoclonus; alkalosis 2 3 Johan den Dunnen
00437038 Pat50 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M no France - - - - - GTLMNS high blood pressure; hypokalemia; metabolic alkalosis 2 1 Johan den Dunnen
00437039 Pat120 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, 1 affected, unaffected parents F - Germany - - - - - GTLMNS pyelonephritis 2 1 Johan den Dunnen
00437040 Pat30 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS hypokalemia 2 1 Johan den Dunnen
00437041 Pat98 PubMed: Viering 2023, Journal: Viering 2023 - M - Germany - - - - - GTLMNS - 2 1 Johan den Dunnen
00437042 Pat103 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected sister, unaffected parents M - Germany - - - - - GTLMNS - 2 2 Johan den Dunnen
00437043 Pat43 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS hypokalemia; asthenia 2 1 Johan den Dunnen
00437044 Pat5 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS hypokalemia; hypochloremia; alkalosis; asthenia 2 1 Johan den Dunnen
00437045 Pat27 PubMed: Viering 2023, Journal: Viering 2023 - M - France - - - - - GTLMNS asymptomatic profound hypokalemia; metabolic alkalosis; hypomagnesemia 2 1 Johan den Dunnen
00437046 Pat17 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and 2 affected sisters, unaffected parents F no France - - - - - GTLMNS hypokalemia 2 3 Johan den Dunnen
00437047 Pat75 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M no France - - - - - GTLMNS hypokalemia; asthenia 2 1 Johan den Dunnen
00437048 Pat37 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS cramps; hypokalemia; 2 1 Johan den Dunnen
00437049 Pat45 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS hypokalemia; faintness 2 1 Johan den Dunnen
00437050 Pat9 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS deterioration of general condition; hypokalemia; polyphagia 2 1 Johan den Dunnen
00437051 Pat111 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, 1 affected, unaffected parents F - Germany - - - - - GTLMNS - 2 1 Johan den Dunnen
00437052 Pat21 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M no France - - - - - GTLMNS hypokalemia 2 1 Johan den Dunnen
00437053 Pat105 PubMed: Viering 2023, Journal: Viering 2023 - F - Germany - - - - - GTLMNS - 2 1 Johan den Dunnen
00437054 Pat118 PubMed: Viering 2023, Journal: Viering 2023 - M - Germany - - - - - GTLMNS incidental finding 2 1 Johan den Dunnen
00437055 Pat121 PubMed: Viering 2023, Journal: Viering 2023 - F - Germany - - - - - GTLMNS - 2 1 Johan den Dunnen
00437056 Pat109 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected sister, unaffected parents M - Germany - - - - - GTLMNS - 2 2 Johan den Dunnen
00437057 Pat122 PubMed: Viering 2023, Journal: Viering 2023 - F - Germany - - - - - GTLMNS - 2 1 Johan den Dunnen
00437058 Pat100 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected sister, unaffected parents F - Germany - - - - - GTLMNS tetany 2 2 Johan den Dunnen
00437059 Pat42 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected brother, unaffected parents F no France - - - - - GTLMNS hypokalemia 2 2 Johan den Dunnen
00437060 Pat31 PubMed: Viering 2023, Journal: Viering 2023 - F - France - - - - - GTLMNS hypokalaemic tubular acidosis; hypomagnesemia; hypermagnesuria 2 1 Johan den Dunnen
00437061 Pat88 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M no France - - - - - GTLMNS malaise; hypokalemia 2 1 Johan den Dunnen
00437062 Pat11 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected sister, unaffected parents F no France - - - - - GTLMNS hypokalemia; faintness; hypomagnesemia; metabolic alkalosis; 2 2 Johan den Dunnen
00437063 Pat93 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS fortuitous hypokalemia 2 1 Johan den Dunnen
00437064 Pat47 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M yes France - - - - - GTLMNS hypokalemia; faintness 2 1 Johan den Dunnen
00437065 Pat99 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected brother, unaffected parents F - Germany - - - - - GTLMNS - 2 2 Johan den Dunnen
00437066 Pat25 PubMed: Viering 2023, Journal: Viering 2023 - F - France - - - - - GTLMNS hypokalemia; metabolic alkalosis; hypomagnesemia; growth failure 2 1 Johan den Dunnen
00437067 Pat64 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected sister, unaffected parents M no France - - - - - GTLMNS hypokalemia 2 2 Johan den Dunnen
00437068 Pat34 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M no France - - - - - GTLMNS hypokalemia; polyarthralgia; asthenia 2 1 Johan den Dunnen
00437069 Pat96 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected brother, unaffected parents F no France - - - - - GTLMNS hypokalemia; asthenia; faintness; tetany 2 2 Johan den Dunnen
00437070 Pat65 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history F no France - - - - - GTLMNS hypokalemia; tetany; abdominal pains; vomiting; convulsion; cardiac arrest 2 1 Johan den Dunnen
00437071 Pat36 PubMed: Viering 2023, Journal: Viering 2023 - M - France - - - - - GTLMNS hypokalemia; alkalosis; hypomagnesemia; chondrocalcinosis 2 1 Johan den Dunnen
00437072 Pat33 PubMed: Viering 2023, Journal: Viering 2023 2-generation family, patient and affected sister, unaffected parents M no France - - - - - GTLMNS tingling of feet and hand; hypokalemia; 2 2 Johan den Dunnen
00437073 Pat58 PubMed: Viering 2023, Journal: Viering 2023 - F - France - - - - - GTLMNS hypokalemia 2 1 Johan den Dunnen
00437074 Pat102 PubMed: Viering 2023, Journal: Viering 2023 - M - Germany - - - - - GTLMNS growth retardation 2 1 Johan den Dunnen
00437075 Pat60 PubMed: Viering 2023, Journal: Viering 2023 - F - France - - - - - GTLMNS hypokalemia 2 1 Johan den Dunnen
00437076 Pat87 PubMed: Viering 2023, Journal: Viering 2023 patient, no family history M no France - - - - - GTLMNS growth failure (-4SD); hypokalemia 2 1 Johan den Dunnen
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