ORPHA:95626
Acquired arginine vasopressin deficiency
Synonyms: Acquired CDI · Acquired neurogenic diabetes insipidus
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Age of onset
- All ages
- Status
- active
A subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia, due to an idiopathic or secondary decrease in vasopressin (AVP) production.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired arginine vasopressin deficiency | Acquired CDI · Acquired neurogenic diabetes insipidus |
| fr | Déficit acquis en arginine vasopressine | DIC acquis · Diabète insipide neurogène acquis |
| de | Arginin-Vasopressin-Mangel, erworbener | CDI, erworbener · Neurogener Diabetes insipidus, erworbener |
| es | Deficiencia de arginina vasopresina adquirida | DIC adquirida · Diabetes insipida central adquirida · Diabetes insipida neurogénica adquirida |
| it | Deficit acquisito di arginina vasopressina | CDI acquisito · Diabete insipido neurogeno acquisito |
| nl | Verworven deficiëntie van arginine-vasopressine | Verworven neurogene diabetes insipidus · Verworven CDI |
| pt | Deficiência de arginina vasopressina adquirida | CDI adquirida · Diabetes insipidus neurogénica adquirida |
| pl | Nabyta moczówka prosta centralna | Nabyta CDI · Nabyta moczówka prosta neurogenna · Nabyty niedobór wazopresyny argininowej |
| cs | Ziskaný centrální diabetes insipidus | Získaný CDI · Získaný neurogenní diabetes insipidus |
| uk | Набутий дефіцит аргінін-вазопресину | Набутий CDI · Набутий нейрогенний нецукровий діабет |
| zh | 获得性中枢性尿崩症 | 获得性神经性尿崩症 |
| tr | Edinsel santral diabetes insipidus | Edinsel CDI · Edinsel nörojenik diabetes insipidus |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E23.2 | NTBT | attributed | validated |
| ICD-11 | 5A61.5 | NTBT | index | validated |
| MONDO | 0019846 | E | validated | |
| UMLS | C5680256 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:178029Arginine vasopressin deficiency
rare endocrine diseases
No children.
Codes that Orphanet moved or referred to this one:
- ORPHA:95625OBSOLETE: Posttraumatic diabetes insipidus referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
4 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000873 | Diabetes insipidus | |
| HP:0100515 | Pollakisuria | |
| HP:0001959 | Polydipsia | |
| Frequent (79-30%) | ||
| HP:0001824 | Weight loss | |
Run the differential on the 3 obligate / very frequent terms
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/95626
- This record as JSON: /data/d/95626.json