Disease #02652

Official abbreviation Bartter-3
Name Bartter syndrome, type 3
OMIM ID 607364
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 7
Phenotype entries for this disease 6
Associated with 1 gene CLCNKB
Associated tissues -
Disease features -
Remarks -


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00080887 - Trujillano et al., submitted unaffected parents - - - - - 0 - - Bartter-3 Bartter syndrome, type 4B (OMIM:607364) CLCNKB CLCNKB 1 1 Daniel Trujillano
00206494 - - - M - Thailand - - 0 - - Bartter-3 - CLCNKB CLCNKB 1 1 Rosa Vargas-Poussou
00206495 - - - - - - - - 0 - - Bartter-3 - CLCNKB CLCNKB 1 1 Damien Bruno
00206496 - - - F yes Turkey - - 0 - - Bartter-3 - CLCNKB CLCNKB 1 1 Rosa Vargas-Poussou
00206497 - - - F no France - - 0 - - Bartter-3 - CLCNKB CLCNKB 2 1 Rosa Vargas-Poussou
00206498 - - - M no Morocco - - 0 - - Bartter-3 - CLCNKB CLCNKB 1 1 Rosa Vargas-Poussou
00206499 - - - M yes Algeria - - 0 - - Bartter-3 - CLCNKB CLCNKB 1 1 Rosa Vargas-Poussou
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