number anomaly of chromosome X in humans (Q20104): Difference between revisions
Jump to navigation
Jump to search
Superraptor (talk | contribs) (Created claim: broader (P104): gonosomal difference in humans (Q20102)) |
Superraptor (talk | contribs) (Changed claim: narrower (P105): Turner syndrome (Q20145)) |
||
(4 intermediate revisions by the same user not shown) | |||
Property / narrower | |||
Property / narrower: Turner syndrome / rank | |||
Normal rank | |||
Property / narrower: Turner syndrome / reference | |||
Property / narrower | |||
Property / narrower: Klinefelter syndrome / rank | |||
Normal rank | |||
Property / narrower: Klinefelter syndrome / reference | |||
Property / ICD-11 Foundation URI | |||
Property / ICD-11 Foundation URI: 1293378897 / rank | |||
Normal rank | |||
Property / ICD-11 to ICD-10 mapping | |||
Property / ICD-11 to ICD-10 mapping: chromosomal difference not elsewhere classified / rank | |||
Normal rank |
Latest revision as of 23:23, 25 April 2024
No description defined
- number anomalies of chromosome X in humans
- number anomaly of chromosome X
- number anomalies of chromosome X
- numeric anomaly of chromosome X
- numeric anomalies of chromosome X
- number anomaly of X chromosomes
- number anomalies of X chromosomes
Language | Label | Description | Also known as |
---|---|---|---|
English | number anomaly of chromosome X in humans |
No description defined |
|