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loading...| Preferred Name |
Klinefelter syndrome |
| Synonyms |
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]. |
| database_cross_reference |
GARD:8705 ICD9CM:758.7 UMLS_CUI:C0022735 MESH:D007713 SNOMEDCT_US_2020_03_01:405770005 ICD10CM:Q98.0 NCI:C34752 |
| has exact synonym |
XXY syndrome Klinefelter's syndrome XXY trisomy Hypogonadotropic Hypogonadism 47, XXY |
| id |
DOID:1921 |
| in_subset | |
| label |
Klinefelter syndrome |
| notation |
DOID:1921 |
| prefLabel |
Klinefelter syndrome |
| textual definition |
A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. |
| 引自 | |
| 有_obo_命名空间 |
disease_ontology |
| subClassOf |
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