Phenotypes for disease #02652 (BARTS3 (Bartter syndrome, type 3 (BARTS3)), OMIM:607364)

11 entries on 1 page. Showing entries 1 - 11.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060456 Bartter syndrome, type 4B (OMIM:607364) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080887
0000154434 - - - Familial, autosomal recessive - - - 5m - Rosa Vargas-Poussou 00206494
0000154435 - - - Familial, autosomal recessive - 6m - - - Rosa Vargas-Poussou 00206496
0000154436 - - - Isolated (sporadic) - 28y - - - Rosa Vargas-Poussou 00206497
0000154437 - - - Isolated (sporadic) - 13y - - - Rosa Vargas-Poussou 00206498
0000154438 - - - Familial, autosomal recessive - 1y - - - Rosa Vargas-Poussou 00206499
0000220901 Salt wasting, hypokalaemia, metabolic alkalosis,Slight reduction of weight growth, vomit, anorexia, dehydration Bartter syndrome Bartter syndrome type 3 Familial, autosomal recessive 00y05m 00y05m 00y05m - - Dr Silvana Tedeschi 00287167
0000220902 salt wasting, hypokalaemia, metabolic alkalosis, Asthenia, polydipsia, cramps, tingling, abdominal pain, polyuria, heart problems, tetany, hyperpyrexia Bartter syndrome Bartter syndrome type 3 Familial, autosomal recessive 23y 23y 23y - - Dr Silvana Tedeschi 00287168
0000220903 salt wasting, hypokalaemia, metabolic alkalosis, Slowing growth, vomit, polyuria, anorexia, iperuricemia Bartter syndrome Bartter syndrome type 3 Familial, autosomal recessive 00y05m - 00y05m 5m - Dr Silvana Tedeschi 00287169
0000220904 salt wasting, hypokalaemia, metabolic alkalosis, Growth delay, polyhydramnios, asthenia Bartter syndrome Bartter syndrome type 3 Familial, autosomal recessive 00y06m - 00y06m 6m - Dr Silvana Tedeschi 00287166
0000242298 - - - Unknown 52y - - - - Takayasu Mori 00320245
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