遗传性癌症易感综合征
Inherited cancer-predisposing syndromes
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- 02 肿瘤
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- 2 级
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- 遗传性乳腺癌-卵巢癌综合征2C65
- 酪氨酸血症1型5C50.11
- Gardner综合征LD2D.3
- 波伊茨-耶格综合征LD2D.0
- 1型神经纤维瘤病LD2D.10
- 2型神经纤维瘤病LD2D.11
- 3型神经纤维瘤病LD2D.12
- 结节性硬化症LD2D.2
- Gorlin综合征LD2D.4
- 着色性干皮病LD27.1
- Noonan综合征LD2F.15
- Blackfan-Diamond贫血3A60.1
- Costello综合征LD2F.1Y
- 家族性多发性脑脊膜瘤2A01.00
- 家族性卵巢癌2C73.Y
- 家族性前列腺癌2C82.Y
- 遗传性乳腺癌2C6Y
- Kostmann综合征4B00.00
- Li-Fraumeni综合征2B51.Y
- 多发性内分泌腺瘤病1型2F7A.0
- 多发性内分泌腺瘤病2型2F7A.0
- 多发性内分泌腺瘤病4型2F7A.0
- N综合征LD2H.Y
- Nijmegen断裂综合征4A01.31
- Nijmegen断裂综合征样疾患4A01.31
- 少牙畸形-癌症易感综合征LD27.0Y
- Perlman综合征2C90.Y
- Schinzel-Giedion综合征LD27.0Y
- Shwachman-Diamond综合征3A70.0
- Silver-Russell综合征LD2F.1Y
- Simpson-Golabi-Behmel综合征LD2C
- Sotos综合征LD2C
- Von Hippel-Lindau病5A75
- WAGR综合征LD2A.Y
- Warsaw断裂综合征LD2F.1Y
- 偏侧肢体肥大LD2C
- Rothmund-Thomson综合征2型LD2B
- Aicardi综合征LD20.Y
- Hashimoto-Pritzker综合征2B31.2Y
- Wiskott-Aldrich综合征3B62.0Y
- 普通变异型免疫缺陷病4A01.0Y
- 家族性血小板综合征伴急性髓性白血病倾向3B62.3
- 蓝色橡皮疱痣综合征LC51
- 内生软骨瘤病2E83.Z
- Saethre-Chotzen综合征LD24.GY
- 家族性腺瘤性息肉病2B90.Y
- 幼年型胃肠道息肉病2B90.Y
- 增生性息肉综合征2E92.40
- 遗传性混合息肉病综合征2E92.40
- 家族性非息肉性结直肠癌2B90.Y
- Alagille综合征LB20.0Y
- Cockayne综合征LD2B
- Werner综合征LD2B
- 大头畸形-毛细血管畸形LD2F.1Y
- Rubinstein-Taybi综合征LD2F.1Y
- Schöpf-Schulz-Passarge综合征LD27.0Y
- McCune-Albright综合征FB80.0
- Bannayan-Riley-Ruvalcaba综合征LD2D.Y
- Cowden综合征LD2D.Y
- Bazex-Dupré-Christol综合征LD27.5
- Bloom综合征4A01.31
- 共济失调-毛细血管扩张症4A01.31
- 共济失调-毛细血管扩张症样疾患4A01.31
- 先天性角化不良3A70.0
- 范可尼贫血3A70.0
- Beckwith-Wiedemann综合征LD2C
- 耳聋-淋巴水肿-白血病综合征BD93.0
- 嵌合非整倍杂色体综合征LD7Y
- Denys-Drash综合征LD2A.Y
- Birt-Hogg-Dubé综合征LD27.5
- 家族性肾细胞癌2C90.0
- 非息肉病性Turcot综合征2A0Z
英文词条（72）
- Hereditary breast and ovarian cancer syndrome2C65
- Tyrosinaemia type 15C50.11
- Gardner syndromeLD2D.3
- Peutz-Jeghers syndromeLD2D.0
- Neurofibromatosis type 1LD2D.10
- Neurofibromatosis type 2LD2D.11
- Neurofibromatosis type 3LD2D.12
- Tuberous sclerosisLD2D.2
- Gorlin syndromeLD2D.4
- Xeroderma pigmentosumLD27.1
- Noonan syndromeLD2F.15
- Blackfan-Diamond anaemia3A60.1
- Costello syndromeLD2F.1Y
- Familial multiple meningioma2A01.00
- Familial ovarian cancer2C73.Y
- Familial prostate cancer2C82.Y
- Hereditary breast cancer2C6Y
- Kostmann syndrome4B00.00
- Li-Fraumeni syndrome2B51.Y
- Multiple endocrine neoplasia type 12F7A.0
- Multiple endocrine neoplasia type 22F7A.0
- Multiple endocrine neoplasia type 42F7A.0
- N syndromeLD2H.Y
- Nijmegen breakage syndrome4A01.31
- Nijmegen breakage syndrome-like disorder4A01.31
- Oligodontia - cancer predisposition syndromeLD27.0Y
- Perlman syndrome2C90.Y
- Schinzel-Giedion syndromeLD27.0Y
- Shwachman-Diamond syndrome3A70.0
- Silver-Russell syndromeLD2F.1Y
- Simpson-Golabi-Behmel syndromeLD2C
- Sotos syndromeLD2C
- Von Hippel-Lindau disease5A75
- WAGR syndromeLD2A.Y
- Warsaw breakage syndromeLD2F.1Y
- HemihypertrophyLD2C
- Rothmund-Thomson syndrome type 2LD2B
- Aicardi syndromeLD20.Y
- Hashimoto-Pritzker syndrome2B31.2Y
- Wiskott-Aldrich syndrome3B62.0Y
- Common variable immunodeficiency4A01.0Y
- Familial platelet syndrome with predisposition to acute myelogenous leukaemia3B62.3
- Blue rubber bleb naevus syndromeLC51
- Enchondromatosis2E83.Z
- Saethre-Chotzen syndromeLD24.GY
- Familial adenomatous polyposis2B90.Y
- Juvenile gastrointestinal polyposis2B90.Y
- Hyperplastic polyposis syndrome2E92.40
- Hereditary mixed polyposis syndrome2E92.40
- Familial nonpolyposis colorectal cancer2B90.Y
- Alagille syndromeLB20.0Y
- Cockayne syndromeLD2B
- Werner syndromeLD2B
- Macrocephaly - capillary malformationLD2F.1Y
- Rubinstein-Taybi syndromeLD2F.1Y
- Schöpf-Schulz-Passarge syndromeLD27.0Y
- McCune-Albright syndromeFB80.0
- Bannayan-Riley-Ruvalcaba syndromeLD2D.Y
- Cowden syndromeLD2D.Y
- Bazex-Dupré-Christol syndromeLD27.5
- Bloom syndrome4A01.31
- Ataxia-telangiectasia4A01.31
- Ataxia-telangiectasia-like disorder4A01.31
- Dyskeratosis congenita3A70.0
- Fanconi anaemia3A70.0
- Beckwith-Wiedemann syndromeLD2C
- Deafness, lymphoedema and leukaemia syndromeBD93.0
- Mosaic variegated aneuploidy syndromeLD7Y
- Denys-Drash syndromeLD2A.Y
- Birt-Hogg-Dubé syndromeLD27.5
- Familial renal cell carcinoma2C90.0
- Nonpolyposis Turcot syndrome2A0Z
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该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。