Post-traumatic pituitary deficiency
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Status
- active
A rare, acquired, endocrine disorder characterized by deficiency of one or more of the pituitary hormones resulting as a consequence of traumatic or medically-induced injury of the pituitary gland. Clinical presentation is variable depending on the nature and acuity of the injury and the resulting order and amount of hormone deficiency.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Post-traumatic pituitary deficiency | |
| fr | Insuffisance hypophysaire d'origine post-traumatique | |
| de | Hypophysenfunktionsstörung, posttraumatische | |
| es | Deficiencia hipofisaria postraumática | |
| it | Deficit ipofisario iatrogeno o traumatico | |
| nl | Posttraumatische hypofysedeficiëntie | |
| pt | Deficiência pituitária pós-traumática | |
| pl | Jatrogenny lub pourazowy Niedobór hormonów przysadki | |
| cs | Iatrogenní nebo traumatický deficit hormonů hypofýzy | |
| uk | Посттравматичний дефіцит гормонів гіпофізу | |
| zh | 创伤后垂体缺陷 | |
| tr | Travma sonrası hipofiz eksikliği |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E23.6 | NTBT | attributed | validated |
| ICD-11 | 5A61.0 | NTBT | attributed | validated |
| MONDO | 0019845 | E | validated | |
| MONDO | 19845 | E | validated | |
| UMLS | C0342400 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:95502Acquired pituitary hormone deficiency
rare endocrine diseases
No children.
Codes that Orphanet moved or referred to this one:
- ORPHA:95621OBSOLETE: Postsurgical hypopituitarism referred to · inactive
- ORPHA:95623OBSOLETE: Posttraumatic hypopituitarism referred to · inactive
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
20 annotations · validated 2017-04-10| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Occasional (29-5%) | ||
| HP:0040086 | Abnormal prolactin level | |
| HP:0000141 | Amenorrhea | |
| HP:0002920 | Decreased circulating ACTH level | |
| HP:0000824 | Decreased response to growth hormone stimulation test | |
| HP:0012378 | Fatigue | |
| HP:0001943 | Hypoglycemia | |
| HP:0000044 | Hypogonadotropic hypogonadism | |
| HP:0002615 | Hypotension | |
| HP:0000789 | Infertility | |
| HP:0000938 | Osteopenia | |
| HP:0005625 | Osteoporosis of vertebrae | |
| Very rare (<4-1%) | ||
| HP:0009888 | Abnormality of secondary sexual hair | |
| HP:0010311 | Aplasia/Hypoplasia of the breasts | |
| HP:0000863 | Central diabetes insipidus | |
| HP:0008734 | Decreased testicular size | |
| HP:0000823 | Delayed puberty | |
| HP:0002750 | Delayed skeletal maturation | |
| HP:0001510 | Growth delay | |
| HP:0000871 | Panhypopituitarism | |
| HP:0008245 | Pituitary hypothyroidism | |
Annotation source: 24635130[PMID]_26307884[PMID]_24243629[PMID]_23690314[PMID]_22090267[PMID]_17895459[PMID]_18234750[PMID]_17467517[PMID]_15472187[PMID]_16378796[PMID]_4301762[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/95619
- This record as JSON: /data/d/95619.json