about
Gitelman syndromeoculocerebrorenal syndromeRHYNS syndromeHUPRA syndromeEAST syndromehereditary renal hypouricemianephrogenic diabetes insipidus-intracranial calcification syndromenephrogenic syndrome of inappropriate antidiuresishypotonia-cystinuria syndrome type 1primary renal tubular acidosismitochondrial DNA depletion syndrome, hepatocerebrorenal form
P279
Q1053120-9876C467-724A-407E-B6C1-0ECB58C3F884Q1200839-61723586-C018-4B4D-8665-4979F8179E59Q19709333-1B4664DD-376B-4CCA-BF7B-938368D760B9Q30314091-52542786-F3C4-4721-92A6-4825DDF39073Q5322531-A9C1323B-6329-49E8-84B0-D52F87CC224EQ55781796-416A5700-2779-4C73-9D49-76DD9AD1CC53Q55781817-6F99BC35-2A0B-41F4-9814-6F4F31E30419Q55782451-D5D8340F-52B3-48A7-BF97-00E0C600FF27Q55786291-339399F8-7AA9-499B-ACE9-DD96F988DCADQ55787422-B3309EE5-F940-43AD-8E78-4B985EA71275Q55787787-CD95C677-F954-4F14-8B63-38A83BDAF0CA
P279
description
human disease
@en
name
inherited renal tubular disease
@en
type
label
inherited renal tubular disease
@en
prefLabel
inherited renal tubular disease
@en
P279
P1550
P2888
P5270
MONDO:0015962