ORPHA:101957
Pituitary deficiency
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pituitary deficiency | |
| fr | Déficit hypophysaire | |
| de | Hypophysenfunktionsstörung | |
| es | Deficiencia hipofisaria | |
| it | Insufficienza ipofisaria | |
| nl | Hypofysedeficiëntie | |
| pt | Deficiência hipofisária | Deficiência da pituitária |
| pl | Niedoczynność przysadki | |
| cs | Pituitární deficit | |
| uk | Гіпофізарний дефіцит | |
| zh | 垂体缺陷 | |
| tr | Hipofiz yetmezliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E23.0 | E | specific | validated |
| ICD-11 | 5A61.0 | E | specific | validated |
| MONDO | 0015127 | E | validated | |
| MONDO | 15127 | E | validated | |
| UMLS | C0020635 | E | validated | |
| GARD | 19801 | 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 (2):
- ORPHA:183628Rare genetic hypothalamic or pituitary disease
rare genetic diseases - ORPHA:181384Rare hypothalamic or pituitary disease
rare endocrine diseases
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/101957
- This record as JSON: /data/d/101957.json