ORPHA:181441
Rare disorder with hypergonadotropic hypogonadism
Synonyms: Rare disorder with primary hypogonadism
- 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 | Rare disorder with hypergonadotropic hypogonadism | Rare disorder with primary hypogonadism |
| fr | Maladie rare avec hypogonadisme hypergonadotrope | Maladie rare avec hypogonadisme primaire |
| de | Seltene Syndrome mit hypergonadotropen Hypogonadismus | Seltene Störung mit primärem Hypogonadismus |
| es | Enfermedad rara con hipogonadismo hipergonadotrópico | Enfermedad rara con hipogonadismo primario |
| it | Disturbo raro con ipogonadismo ipergonadotropo | Disturbo raro con ipogonadismo primitivo |
| nl | Zeldzame stoornis met hypergonadotroop hypogonadisme | Zeldzame stoornis met primair hypogonadisme |
| pt | Doença rara com hipogonadismo hipergonadotrópico | Doença rara com hipogonadismo primário |
| pl | Rzadka choroba z hipogonadyzmem hipergonadotropowym | Rzadka choroba z hipogonadyzmem pierwotnym |
| cs | Vzácná onemocnění s hypergonadotropním hypogonadismem | Vzácná onemocnění s primárním hypogonadismem |
| uk | Рідкісний розлад з гіпергонадотропним гіпогонадизмом | Рідкісний розлад з первинним гіпогонадизмом |
| zh | 罕见病伴性腺功能减退症 | 伴原发性性腺机能减退的罕见病 |
| tr | Hipergonadotropik hipogonadizm ile seyreden nadir bozukluk | Primer hipogonadizm ile nadir bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15906 | E | validated | |
| UMLS | C5679596 | 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:97978Rare endocrine disease
rare endocrine diseases - ORPHA:156638Rare genetic endocrine disease
rare genetic diseases - ORPHA:399685Rare male infertility due to testicular endocrine disorder
rare genetic diseases; rare infertility disorders
Children (16):
- ORPHA:90646Deafness-hypogonadism syndrome
- ORPHA:2229Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
- ORPHA:2183Hydrocephalus-obesity-hypogonadism syndrome
- ORPHA:2410Hypergonadotropic hypogonadism-cataract syndrome
- ORPHA:2233Hypogonadism-mitral valve prolapse-intellectual disability syndrome
- ORPHA:3044Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome
- ORPHA:2234Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome
- ORPHA:2558Mikati-Najjar-Sahli syndrome
- ORPHA:280679Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome
- ORPHA:648Noonan syndrome
- ORPHA:2232Primary hypergonadotropic hypogonadism-partial alopecia syndrome
- ORPHA:606Proximal myotonic myopathy
- ORPHA:3464Woodhouse-Sakati syndrome
- ORPHA:43X-linked adrenoleukodystrophy
- ORPHA:163971X-linked intellectual disability, Cilliers type
- ORPHA:163976X-linked intellectual disability, Van Esch type
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/181441
- This record as JSON: /data/d/181441.json