ORPHA:95488
Non-acquired pituitary hormone 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 | Non-acquired pituitary hormone deficiency | |
| fr | Insuffisance hypophysaire non acquise | |
| de | Hypophysenhormon-Mangel, nicht erworbener | |
| es | Deficiencia no adquirida de hormonas hipofisarias | |
| it | Deficit non acquisito degli ormoni pituitari | |
| nl | Niet-verworven hypofysehormoondeficiëntie | |
| pt | Deficiência de hormona pituitária não-adquirida | |
| pl | Wrodzony Niedobór hormonów przysadki | |
| cs | Nezískaný deficit hypofyzárních hormonů | |
| uk | Ненабутий дефіцит гормонів гіпофіза | |
| zh | 非获得性垂体激素缺乏症 | |
| tr | Edinsel olmayan hipofiz hormonu eksikliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019824 | E | validated | |
| UMLS | C5681572 | 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 (3):
- ORPHA:156643Genetic endocrine growth disease
rare genetic diseases - ORPHA:101957Pituitary deficiency
rare genetic diseases; rare endocrine diseases - ORPHA:90692Rare endocrine growth disease
rare endocrine diseases
Children (7):
- ORPHA:174590Congenital hypogonadotropic hypogonadism
- ORPHA:199296Congenital isolated ACTH deficiency
- ORPHA:90674Isolated thyroid-stimulating hormone deficiency
- ORPHA:467Non-acquired combined pituitary hormone deficiency
- ORPHA:631Non-acquired isolated growth hormone deficiency
- ORPHA:95496Pituitary stalk interruption syndrome
- ORPHA:314811Short stature due to GHSR deficiency
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/95488
- This record as JSON: /data/d/95488.json