ORPHA:238305
Infundibulo-neurohypophysitis
- Type
- Disease
- Group
- Disorder
- Status
- active
A type of primary hypophysitis characterized by an inflammation of the posterior pituitary and the stalk. The major clinical manifestation is diabetes insipidus with polyuria and polydipsia. Less frequent symptoms are headaches, adrenal insufficiency, hyperprolactinemia and hypogonadism.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infundibulo-neurohypophysitis | |
| fr | Neurohypophysite infundibulaire | |
| de | Infundibuloneurohypophysitis | |
| es | Infundibulo-neurohipofisitis | |
| it | Neuroipofisite infundibulare | |
| nl | Infundibulo-neurohypofysitis | |
| pt | Infundibulo-neuro-hipofisite | |
| pl | Zapalenie części nerwowej i szypuły przysadki | |
| cs | Autoimunitní hypofyzitida | |
| uk | Інфундибуло-нейрогіпофізит | |
| zh | 漏斗神经下垂体炎 | |
| tr | Infundibulo-nörohipofizit |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E23.6 | NTBT | attributed | validated |
| ICD-11 | 5A61.5 | NTBT | index | validated |
| MONDO | 0016534 | E | validated | |
| UMLS | C5190834 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:95506Primary hypophysitis
rare endocrine diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/238305
- This record as JSON: /data/d/238305.json