nephrogenic diabetes insipidus
Information
- Disease name
- nephrogenic diabetes insipidus
- Disease ID
- DOID:12387
- Description
- "A diabetes insipidus that is characterized by a complete or partial resistance of the kidneys to vasopressin (ADH)." [url:http\://en.wikipedia.org/wiki/Nephrogenic_diabetes_insipidus, url:http\://ghr.nlm.nih.gov/condition/nephrogenic-diabetes-insipidus, url:https\://medlineplus.gov/ency/article/000511.htm]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00478335 | Completed | N/A | Pharmacologic Treatment of Congenital Nephrogenic Diabetes Insipidus | May 2007 | October 2012 |
| NCT04939753 | Completed | Nephrogenic Diabetes Insipidus During Prolonged Sevoflurane Sedation in the ICU: a Retrospective Analysis | May 26, 2021 | April 1, 2023 | |
| NCT05190744 | Recruiting | Phase 2 | PB to Treat Hereditary Nephrogenic Diabetes Insipidus, ADPKD Treated With Tolvaptan, and Severely Polyuric Patients With Previous Lithium Administration | September 1, 2022 | December 31, 2025 |
| NCT06065852 | Recruiting | National Registry of Rare Kidney Diseases | November 6, 2009 | December 31, 2039 | |
| NCT05307042 | Unknown status | Decline in Renal Concentration Ability in Lithium Treated Patients | May 2022 | December 2022 |
- Disase is a (Disease Ontology)
- DOID:9409
- Cross Reference ID (Disease Ontology)
- GARD:7178
- Cross Reference ID (Disease Ontology)
- ICD10CM:N25.1
- Cross Reference ID (Disease Ontology)
- ICD9CM:588.1
- Cross Reference ID (Disease Ontology)
- MESH:D018500
- Cross Reference ID (Disease Ontology)
- NCI:C84919
- Cross Reference ID (Disease Ontology)
- ORDO:223
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:123294004
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0162283
- Disase Synonym (Disease Ontology)
- vasopressin-resistant diabetes insipidus
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0009806
- OrphaNumber from OrphaNet (Orphanet)
- 223
- MedGen concept unique identifier (MedGen Concept name)
- C0162283
- MedGen unique identifier (MedGen Concept name)
- 57876
- ICD10 preferred id (Insert disease from ICD10)
- D0011283
- ICD10 class code (Insert disease from ICD10)
- N25.1