ORPHA:156643
Genetic endocrine growth disease
- 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 | Genetic endocrine growth disease | |
| fr | Maladie endocrinienne génétique de la croissance | |
| de | Wachstumsstörung, endokrine, genetisch bedingte | |
| es | Enfermedad endocrina genética del crecimiento | |
| it | Malattia endocrina della crescita, tipo genetico | |
| nl | Genetische endocriene groeiziekte | |
| pt | Doença endócrina do crescimento, genética | |
| pl | Genetyczna endokrynologiczna choroba wzrostu | |
| cs | Geneticky podmíněná endokrinní porucha růstu | |
| uk | Генетично обумовлене ендокринне захворювання росту | |
| zh | 遗传性内分泌生生长疾病 | |
| tr | Genetik endokrin büyüme hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15514 | E | validated | |
| UMLS | C5680637 | 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:156638Rare genetic endocrine disease
rare genetic diseases
Children (10):
- ORPHA:436174Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome
- ORPHA:418Congenital adrenal hyperplasia
- ORPHA:54595Craniopharyngioma
- ORPHA:435554Genetic precocious puberty
- ORPHA:181393Growth hormone insensitivity syndrome
- ORPHA:85173IMAGe syndrome
- ORPHA:494433MIRAGE syndrome
- ORPHA:95488Non-acquired pituitary hormone deficiency
- ORPHA:226292Permanent congenital hypothyroidism
- ORPHA:95709Rare acquired premature ovarian failure
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/156643
- This record as JSON: /data/d/156643.json