loading...| Preferred Name | Klinefelter syndrome | |
| Synonyms |
Klinefelter's syndrome 47, XXY XXY trisomy Hypogonadotropic Hypogonadism XXY syndrome |
|
| Definitions |
A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. No OMIM mapping, confirmed by DO. [LS]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_1921 |
|
| comment |
No OMIM mapping, confirmed by DO. [LS]. |
|
| alternative label |
Klinefelter's syndrome 47, XXY XXY trisomy Hypogonadotropic Hypogonadism XXY syndrome |
|
| database_cross_reference |
MESH:D007713 ICD10CM:Q98.0 UMLS_CUI:C0022735 SNOMEDCT_US_2023_03_01:405770005 ICD9CM:758.7 GARD:8705 NCI:C34752 |
|
| definition |
A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. |
|
| has exact synonym |
Klinefelter's syndrome 47, XXY XXY trisomy Hypogonadotropic Hypogonadism XXY syndrome |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:1921 |
|
| in_subset | ||
| label |
Klinefelter syndrome |
|
| notation |
DOID:1921 |
|
| prefLabel |
Klinefelter syndrome |
|
| subClassOf |