ORPHA:399685
Rare male infertility due to testicular endocrine disorder
- 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 male infertility due to testicular endocrine disorder | |
| fr | Infertilité masculine rare due à un trouble testiculaire endocrine | |
| de | Seltene Form der männlichen Infertilität durch endokrine testikuläre Störung | |
| es | Infertilidad masculina rara por un trastorno endocrino testicular | |
| it | Sterilità maschile rara da disfunzione endocrina testicolare | |
| nl | Zeldzame mannelijke onvruchtbaarheid door testiculaire endocriene stoornis | |
| pt | Infertilidade masculina rara devido a doença endócrina testicular | |
| pl | Rzadka niepłodność męska z powodu endokrynowych zaburzeń jąder | |
| cs | Vzácná mužská neplodnost způsobená testikulární endokrinní poruchou | |
| uk | Рідкісне чоловіче безпліддя, зумовлене ендокринним розладом яєчок | |
| zh | 睾丸内分泌失调所致罕见男性不育 | |
| tr | Testiküler endokrin bozukluğuna bağlı nadir erkek infertilitesi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18388 | E | validated | |
| UMLS | C5681163 | 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:399572Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder
rare infertility disorders - ORPHA:399983Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
rare genetic diseases
Children (6):
- ORPHA:75246,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- ORPHA:75346,XY difference of sex development due to 5-alpha-reductase 2 deficiency
- ORPHA:754Androgen insensitivity syndrome
- ORPHA:481Kennedy disease
- ORPHA:755Leydig cell hypoplasia
- ORPHA:181441Rare disorder with hypergonadotropic hypogonadism
Codes that Orphanet moved or referred to this one:
- ORPHA:98312OBSOLETE: Male infertility with impaired virilization due to a testicular disorder referred to · inactive
- ORPHA:98330OBSOLETE: Male infertility with normal virilization due to androgen administration referred to · inactive
- ORPHA:98331OBSOLETE: Male infertility with normal virilization due to a testicular defect referred to · inactive
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/399685
- This record as JSON: /data/d/399685.json