ORPHA:181402
Syndrome with hypoparathyroidism
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndrome with hypoparathyroidism | |
| fr | Syndrome avec hypoparathyroïdie | |
| de | Syndrom mit Hypoparathyreoidismus | |
| es | Síndrome con hipoparatiroidismo | |
| it | Malattia associata ad ipoparatiroidismo | |
| nl | Syndroom met hypoparathyreoïdie | |
| pt | Síndrome com hipoparatiroidismo | |
| pl | Zespół z niedoczynnością przytarczyc | |
| cs | Syndromy s hypoparatyreoidismem | |
| uk | Синдром гіпопаратиреозу | |
| zh | 伴甲状旁腺功能减退的综合征 | |
| tr | Hipoparatiroidi ile seyreden sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15895 | E | validated | |
| UMLS | C5680611 | 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:208593Genetic hypoparathyroidism
rare genetic diseases - ORPHA:181405Rare hypoparathyroidism
rare endocrine diseases
Children (9):
- ORPHA:56722q11.2 deletion syndrome
- ORPHA:589856Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome
- ORPHA:1563Dahlberg-Borer-Newcomer syndrome
- ORPHA:2237Hypoparathyroidism-sensorineural deafness-renal disease syndrome
- ORPHA:480Kearns-Sayre syndrome
- ORPHA:2333Kenny-Caffey syndrome
- ORPHA:5Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- ORPHA:699Pearson syndrome
- ORPHA:2323Sanjad-Sakati syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/181402
- This record as JSON: /data/d/181402.json