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Karyotype 46,X with abnormal sex chromosome Turner (Q96.200) 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.
Karyotype 46,X isochromosome Xq Turner (Q96.100) 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.
Karyotype 45,X Turner (Q96.000) 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.
Balanced rearrangement (Q95.900) 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 balanced rearrangement (Q95.800) 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.
Individual with autosomal fragile site (Q95.500) 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.
Individual with marker heterochromatin (Q95.400) 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.
Balanced sex/autosomal rearrangement in abnormal individual (Q95.300) 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 compi
Balanced autosomal rearrangement in abnormal individual (Q95.200) 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.
Chromosomal inversion in normal individual (Q95.100) 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.
Balanced translocation in normal individual (Q95.000) 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.
Autosomal deletion (Q93.900) 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 autosomal deletion (Q93.800) 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.
Autosomal deletion with complex rearrangement (Q93.700) 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.
Autosomal deletion (Q93.600) 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.
Angelman syndrome (Q93.501) 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.
Chromosome 22 deletion syndrome (Q93.500x001) 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 partial chromosome deletion (Q93.500) 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.
Cri du chat syndrome (Q93.400x001) 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.
Chromosome 5 short arm deletion (Q93.400) 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.
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