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Male with structurally abnormal sex chromosome (Q98.600) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Karyotype 47,XYY (Q98.500) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Other male with 46,XX karyotype (Q98.300) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Klinefelter male with 46,XX karyotype (Q98.200) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Klinefelter male with >2 X chromosomes (Q98.100) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Klinefelter karyotype 47,XXY (Q98.000) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Sex chromosome abnormality female phenotype (Q97.900) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Other specified sex chromosome abnormality female phenotype (Q97.800) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compi
XY pure gonadal dysgenesis (Q97.300x001) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Female with 46,XY karyotype (Q97.300) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Mosaic with varying X chromosome count (Q97.200) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Female with >3 X chromosomes (Q97.100) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
47,XXX syndrome (Q97.000x001) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Karyotype 47,XXX (Q97.000) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Male gonadal dysgenesis (Q96.901) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Mixed gonadal dysgenesis (Q96.900x002) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Turner syndrome (Q96.900) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Other Turner variant (Q96.800) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Mosaic 45,X/other cell line Turner (Q96.400) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Mosaic 45,X/46,XX or XY Turner (Q96.300) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
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