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Monogenic/syndromic obesity; children.
遗传病科Long QT + deafness; children.
遗传病科Inherited disorders overview; genetics.
遗传病科Trisomy 21; developmental delay; children.
遗传病科Werner syndrome is adult progeria; AR; cataracts; scleroderma-like; cancer.
遗传病科Chromosome abnormality is numerical/structural chromosomal disorder, causing various syndromes. Genetic counseling is used.
遗传病科Sexual development disorder (Q99.801) 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 chromosome abnormality (Q99.800) 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.
Fragile X chromosome (Q99.200) 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.
Pure gonadal dysgenesis (Q99.102) 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.
Pure gonadal dysgenesis (Q99.101) 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.
46,XY DSD (Q99.100x003) 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.
46,XX DSD (Q99.100x002) 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.
46,XX true hermaphrodite (Q99.100) 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.
Sex reversal syndrome (Q99.001) 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.
46,XX male syndrome (Q99.000x001) 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.
Chimera 46,XX/46,XY (Q99.000) 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 male phenotype (Q98.900) 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 male phenotype (Q98.800) 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 compile
Male with sex chromosome mosaic (Q98.700) 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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