ORPHA:95495
Disease associated with non-acquired combined 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 | Disease associated with non-acquired combined pituitary hormone deficiency | |
| fr | Maladie associée à une insuffisance hypophysaire multiple non acquise | |
| de | Hypophysenhormon-Mangel, nicht erworbener, kombinierter, mit assoziierten Fehlbildungen | |
| es | Enfermedad asociada a una deficiencia combinada de hormonas hipofisarias no adquirido | |
| it | Malattia associata a deficit combinato degli ormoni ipofisari non acquisito | |
| nl | Ziekte geassocieerd met niet-verworven gecombineerde hypofysehormoondeficiëntie | |
| pt | Doença associada a deficiência de hormona pituitária combinada não-adquirida | |
| pl | Choroba związana z wrodzonym złożonym niedoborem hormonów tarczycy | |
| cs | Onemocnění asociované s nezískaným kombinovaným deficitem hormonů hypofýzy | |
| uk | Захворювання, повязані з ненабутим комбінованим дефіцитом гормонів гіпофіза | |
| zh | 非获得性联合垂体激素缺乏症相关疾病 | |
| tr | Edinsel olmayan kombine hipofiz hormonu eksikliği ile ilişkili hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681573 | 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:467Non-acquired combined pituitary hormone deficiency
rare genetic diseases; rare endocrine diseases
Children (11):
- ORPHA:157954ANE syndrome
- ORPHA:77298Anophthalmia/microphthalmia-esophageal atresia syndrome
- ORPHA:782Axenfeld-Rieger syndrome
- ORPHA:293978Deficiency in anterior pituitary function-variable immunodeficiency syndrome
- ORPHA:2162Holoprosencephaly
- ORPHA:2315Johanson-Blizzard syndrome
- ORPHA:231720Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome
- ORPHA:672Pallister-Hall syndrome
- ORPHA:420584Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
- ORPHA:3157Septo-optic dysplasia spectrum
- ORPHA:85442Short stature-pituitary and cerebellar defects-small sella turcica syndrome
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/95495
- This record as JSON: /data/d/95495.json