Klinefelter Syndrome
Disease ID: disease_node_4521
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| Dbxref | GARD:8705, ICD10CM:Q98.0, ICD9CM:758.7, MESH:D007713, NCI:C34752, SNOMEDCT_US_2023_03_01:405770005, UMLS_CUI:C0022735 |
|---|---|
| Subclassof | DOID_0060429 |
| Data Source | DOID, MESH |
| Synonyms | 47, XXY, Hypogonadotropic Hypogonadism, Klinefelter's syndrome, XXY syndrome, XXY trisomy |
| Mesh Id | D007713 |
| Mesh Label | Klinefelter Syndrome |
| Mesh Subclassof | D058533, D007006 |
| Doid Label | Klinefelter syndrome |
| Doid Description | 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]. |
| Disease Node Id | disease_node_4521 |
| Doid Id | DOID_1921 |
| Label | Klinefelter Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Duplication Syndrome(ID:disease_node_13621) (Disease)