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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:nephrogenic diabetes insipidus
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Accession:DOID:12387 term browser browse the term
Definition:A genetic or acquired polyuric disorder characterized by persistent hypotonic urine and HYPOKALEMIA. This condition is due to renal tubular insensitivity to VASOPRESSIN and failure to reduce urine volume. It may be the result of mutations of genes encoding VASOPRESSIN RECEPTORS or AQUAPORIN-2; KIDNEY DISEASES; adverse drug effects; or complications from PREGNANCY.
Synonyms:exact_synonym: ADH-Resistant Diabetes Insipidus;   Congenital Nephrogenic Diabetes Insipidus;   Diabetes Insipidus Renalis;   Diabetes Insipidus, Nephrogenic, Autosomal;   Diabetes Insipidus, Nephrogenic, Type 1;   Diabetes Insipidus, Nephrogenic, X-Linked;   NDI;   Nephrogenic Diabetes Insipidus, Type I;   Nephrogenic Diabetes Insipidus, Type II;   XNDI;   acquired nephrogenic diabetes insipidus;   vasopressin-resistant diabetes insipidus
 primary_id: MESH:D018500
 alt_id: OMIM:125800;   OMIM:304800
 xref: GARD:7178;   ICD10CM:N25.1;   ICD9CM:588.1;   NCI:C84919;   ORDO:223
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
nephrogenic diabetes insipidus term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Akr1b1 aldo-keto reductase family 1 member B ISO RGD PMID:10913167 RGD:8548674 NCBI chr 4:61,706,866...61,720,959
Ensembl chr 4:61,706,864...61,720,956
JBrowse link
G Aqp2 aquaporin 2 ISO
DNA, protein:mutation, decreased activity::p.V71M (human)
ClinVar Annotator: match by term: Diabetes insipidus, nephrogenic, autosomal recessive
ClinVar Annotator: match by term: Nephrogenic diabetes insipidus
ClinVar Annotator: match by term: Nephrogenic diabetes insipidus, autosomal
ClinVar Annotator: match by term: Diabetes insipidus, nephrogenic, autosomal dominant
CTD Direct Evidence: marker/mechanism|therapeutic
ClinVar Annotator: match by synonym: Vasopressin-resistant diabetes insipidus
DNA,protein:mutation, altered localization: :p.R254Q(human)
DNA, protein:mutation, altered localization, decreased activity:kidney:p.D150E,G196D(human)
protein:altered localization:kidney
DNA, protein:mutation,decreased secretion: :p.S216F(human)
protein:decreased expression:inner renal medulla collecting duct
DNA, protein:mutation, altered localization: :p.E258K(human)
protein:decreased activity:kidney
PMID:7524315, PMID:7537761, PMID:8140421, PMID:8793791, PMID:9048343, PMID:9302264, PMID:9550615, PMID:9593782, PMID:9649557, PMID:9745427, PMID:10564236, PMID:10574954, PMID:10770218, PMID:10997928, PMID:11076974, PMID:11143979, PMID:11374071, PMID:11536078, PMID:11853799, PMID:11929850, PMID:12050236, PMID:12191971, PMID:14593099, PMID:15509592, PMID:16120822, PMID:16121255, PMID:16361827, PMID:17192724, PMID:18431594, PMID:18470935, PMID:18653713, PMID:18854434, PMID:19293543, PMID:19458121, PMID:20374732, PMID:22644838, PMID:22778181, PMID:25741868, PMID:26467025, PMID:27641679, PMID:28492532, PMID:30784238, PMID:19147915, PMID:11035038, PMID:12191971, PMID:16434568, PMID:16845277, PMID:19585583, PMID:19458121, PMID:16968783, PMID:19461158, PMID:18296634, PMID:18653713, PMID:19701945, PMID:19293543, PMID:17229678 RGD:2314285, RGD:734596, RGD:2314344, RGD:2314325, RGD:2314306, RGD:2314280, RGD:2314282, RGD:2314303, RGD:2314281, RGD:2314293, RGD:2314292, RGD:2314279, RGD:2314283, RGD:2314296 NCBI chr 7:141,237,802...141,242,837
Ensembl chr 7:141,237,768...141,245,165
JBrowse link
G Aqp3 aquaporin 3 (Gill blood group) ISS OMIM:125800 | OMIM:304800 MouseDO NCBI chr 5:57,423,735...57,429,252
Ensembl chr 5:57,423,734...57,429,245
JBrowse link
G Avpr2 arginine vasopressin receptor 2 ISO DNA:deletion, missense mutation, nonsense mutation:p.W296X, p.V88M (human)
ClinVar Annotator: match by term: Nephrogenic diabetes insipidus, X-linked
ClinVar Annotator: match by OMIM:304800
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by synonym: Vasopressin-resistant diabetes insipidus
DNA:mutation:exon:1454C>A (p.S329R) (human)
DNA:deletion (human)
DNA:mutations: :multiple (human)
DNA:missense mutation: :c.262G>A (p.V88M) (human)
DNA:missense mutations: :multiple (human)
PMID:1303257, PMID:1303271, PMID:1356229, PMID:4886456, PMID:5309332, PMID:7541187, PMID:7714087, PMID:7833930, PMID:7913579, PMID:7933835, PMID:7989330, PMID:8037205, PMID:8078903, PMID:8104196, PMID:8401502, PMID:8479490, PMID:8479491, PMID:8704106, PMID:8766931, PMID:8815789, PMID:9027323, PMID:9171234, PMID:9329382, PMID:9369448, PMID:9402087, PMID:9452109, PMID:9587067, PMID:9711877, PMID:9773787, PMID:9853256, PMID:10026829, PMID:10477148, PMID:10714359, PMID:10749568, PMID:10770218, PMID:10820167, PMID:10820168, PMID:10918636, PMID:11128419, PMID:11134505, PMID:11232028, PMID:12414899, PMID:12955588, PMID:14998935, PMID:15129813, PMID:15522100, PMID:15841479, PMID:15872203, PMID:16319185, PMID:16502494, PMID:16689923, PMID:17216256, PMID:17491025, PMID:18407239, PMID:18584216, PMID:18726898, PMID:19703807, PMID:19729439, PMID:19729836, PMID:19812297, PMID:20374732, PMID:20403097, PMID:20459358, PMID:22386940, PMID:22427315, PMID:22644838, PMID:24033266, PMID:25741868, PMID:26077742, PMID:26131744, PMID:26467025, PMID:28492532, PMID:17550212, PMID:17941907, PMID:18489790, PMID:17020465, PMID:19816050, PMID:17371330 RGD:2314017, RGD:2314016, RGD:2314015, RGD:2314019, RGD:2314013, RGD:2314018 NCBI chr  X:156,889,006...156,892,707
Ensembl chr  X:156,889,410...156,891,213
JBrowse link
G Clcnka chloride voltage-gated channel Ka ISO
OMIM:125800 | OMIM:304800 MouseDO PMID:9916798 RGD:1300296 NCBI chr 5:159,931,497...159,946,483
Ensembl chr 5:159,931,511...159,946,446
JBrowse link
G Grn granulin precursor ISS OMIM:125800 | OMIM:304800 MouseDO NCBI chr10:90,377,103...90,383,207
Ensembl chr10:90,376,933...90,383,205
JBrowse link
G Prkca protein kinase C, alpha ISO CTD Direct Evidence: marker/mechanism CTD PMID:25006961 NCBI chr10:96,186,509...96,585,168
Ensembl chr10:96,191,133...96,584,947
JBrowse link
G Ptger4 prostaglandin E receptor 4 treatment ISO RGD PMID:19729836 RGD:10003043 NCBI chr 2:54,951,625...54,966,470
Ensembl chr 2:54,952,821...54,963,448
JBrowse link
G Rnf40 ring finger protein 40 IEP protein:increased expression:kidney (rat) RGD PMID:21734099 RGD:9587431 NCBI chr 1:199,037,472...199,052,823
Ensembl chr 1:199,037,544...199,052,172
JBrowse link
G Sirt1 sirtuin 1 ISS OMIM:125800 | OMIM:304800 MouseDO NCBI chr20:26,831,971...26,851,587
Ensembl chr20:26,833,357...26,852,199
JBrowse link
G Slc4a4 solute carrier family 4 member 4 IDA protein:increased expression:kidney cortex RGD PMID:12944321 RGD:1600034 NCBI chr14:20,476,258...20,817,042
Ensembl chr14:20,479,323...20,920,286
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16096
    disease of anatomical entity 15346
      Urogenital Diseases 4143
        urinary system disease 2066
          kidney disease 1854
            nephrogenic diabetes insipidus 11
              Nephrogenic Diabetes Insipidus with Mental Retardation and Intracerebral Calcification 0
Path 2
Term Annotations click to browse term
  disease 16096
    disease of anatomical entity 15346
      nervous system disease 10864
        central nervous system disease 9008
          brain disease 8328
            thalamic disease 191
              hypothalamic disease 191
                pituitary gland disease 146
                  diabetes insipidus 22
                    nephrogenic diabetes insipidus 11
                      Nephrogenic Diabetes Insipidus with Mental Retardation and Intracerebral Calcification 0
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.