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sex chromosome aneuploidy where a female has three additional X chromosomes
External resources
| Freebase ID | |
| Microsoft Academic ID | |
| Google Knowledge Graph ID | |
| Mondo ID | |
| ICD-10-CM | |
| UMLS CUI | C2937419[2]mapping relation type: close match C0265497[2]mapping relation type: përputhje e përpiktë |
| GARD rare disease ID | |
| ICD-10 | |
| Miraheze article ID | |
| DiseasesDB | |
| ICD-11 (foundation) | |
| APA Dictionary of Psychology entry | |
| Orphanet ID | 11[2]mapping relation type: përputhje e përpiktë |
| MeSH descriptor ID | C535319[2]mapping relation type: përputhje e përpiktë |
| WikiProjectMed ID | |
instancë e
rare disease
chromosomal disease
developmental defect during embryogenesis[2] class of disease
nënklasë e
sex chromosome disorder
Polysomy of X chromosome[2] health specialty
medical genetics
NCI Thesaurus ID
C89802[2]mapping relation type: përputhje e përpiktë
Reference
- ^ Freebase Data Dumps, 28 tetor 2013
- ^ a b c d e f g h Monarch Disease Ontology release 2018-06-29, 28 korrik 2018, MONDO_0015228
- ^ Genetic and Rare Diseases Information Center, 29 mars 2019
