Q929 | »ó¼¼ºÒ¸íÀÇ º¸Åë¿°»öüÀÇ »ï¿°»öüÁõ ¹× ºÎºÐ»ï¿°»öüÁõ | Trisomy and partial trisomy of ther autosomes, unspecified |
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Q93 | ´Þ¸® ºÐ·ùµÇÁö ¾ÊÀº º¸Åë¿°»öüÀÇ ´ÜÀÏ¿°»öüÁõ ¹× °á¼Õ | Monosomies and deletions from the autosomes, NEC |
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Q930 | ¸ðµç ¿°»öüÀÇ ´ÜÀÏ¿°»öüÁõ, °¨¼öºÐ¿ºñºÐ¸® | Whole chromosome monosomy, meiotic nondisjunction |
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Q931 | ¸ðµç ¿°»öüÀÇ ´ÜÀÏ¿°»öüÁõ, ¼¯ÀÓÁõ(À¯»çºÐ¿ºñºÐ¸®) | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
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Q932 | °í¸®¸ð¾ç ¶Ç´Â ½ÖÁß½ÉÀý¿°»öü°¡ ´ëÄ¡µÈ °æ¿ì | Chromosome replaced with ring or dicentric |
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Q933 | 4¹ø ¿°»öü ´Ü¿ÏÀÇ °á¼Õ | Deletion of short arm of chromosome4 |
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Q933 | ¿ùÇÁ-Ç㽬ȣ¸¥ÁõÈıº | Wolff-Hirschorn syndrome |
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Q934 | 5¹ø ¿°»öü ´Ü¿ÏÀÇ °á¼Õ | Deletion of short arm of chromosome 5 |
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Q934 | °í¾çÀÌ¿ïÀ½ ÁõÈıº | Cri-du-chat syndrome |
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Q935 | ¿°»öüÀÇ ±âŸ ºÎºÐ °á¼Õ | Other deletions of part of a chromosome |
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Q935 | ¿£Á©¸¸ ÁõÈıº | Angelman syndrome |
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Q935 | ijÃë22ÁõÈıº | CATCH22 syndrome |
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Q936 | ÀüÁ߱⿡¸¸ º¸ÀÌ´Â °á¼Õ | Deletions seen only at prometaphase |
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Q937 | ±âŸ º¹ÇÕ Àç¹è¿À» µ¿¹ÝÇÑ °á¼Õ | Deletions with other complex rearrangements |
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Q938 | ±âŸ º¸Åë¿°»öüÀÇ °á¼Õ | Other deletions from the autosomes |
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Q939 | »ó¼¼ºÒ¸íÀÇ º¸Åë¿°»öüÀÇ °á¼Õ | Deletions from autosomes, unspecified |
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Q95 | ´Þ¸® ºÐ·ùµÇÁö ¾ÊÀº ±ÕÇü Àç¹è¿ ¹× ±¸Á¶Ç¥ÁöÀÚ | Balanced rearrangements and structural markers, NEC |
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Q95 | ·Î¹öÆ®½¼ ¹× ±ÕÇüÀüÀ§ ¹× »ðÀÔ | Robertsonian and balanced reciprocal translocations and insertions |
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Q950 | Á¤»ó°³Ã¼¿¡¼ÀÇ ±ÕÇü ÀüÀ§ ¹× »ðÀÔ | Balanced translocation and insertion in normal individual |
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Q951 | Á¤»ó°³Ã¼¿¡¼ÀÇ ¿°»öü¿ªÀ§ | Chromosome inversion in normal individual |
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