LD2F.1
非环境引起的多发性结构异常综合征
Syndromes with multiple structural anomalies, not of environmental origin
- 层级
- 4 级
跨章引用 同一概念在其他章节另有编码
- Fraser综合征LD2H.0
- Waardenburg-Shah综合征LD2H.3
- 眼脑肾综合征5C60.0
- 白化病-黑发-肠道神经细胞迁移疾患-感音神经性聋LD2H.Y
- Bardet-Biedl综合征5A61.0
- 眼睑-唇-牙综合征LD27.0Y
- 猫眼综合征LD41.P
- 白内障-智力缺陷-性腺功能减退症5A61.0
- CHARGE综合征5A61.0
- Coffin-Siris综合征LD27.0Y
- Dubowitz综合征LD27.0Y
- 外胚层发育不良-先天性缺指-黄斑营养不良LD27.0Y
- 先天性缺指-外胚层发育不良-唇裂或腭裂LD27.0Y
- 先天性缺指-外胚层发育不良，不伴唇腭裂LD27.0Y
- 先天性巨结肠-聋-多指（多趾）畸形LD2H.Y
- 肢体乳腺综合征LD27.0Y
- Marshall综合征LD27.0Y
- MODY5型综合征5A13.6
- Nijmegen断裂综合征样疾患4A01.31
- Papillorenal综合征LA13.7Y
- Perrault综合征LD2H.Y
- 海豹肢-先天缺指(趾)-耳聋-窦性心律失常LD2H.Y
- Shwachman-Diamond综合征3A70.0
- Smith-Magenis综合征LD44.H1
- 分裂手-分裂足-耳聋LD2H.Y
- 三A综合征5A74.Y
- Waardenburg综合征EC23.2Y
- WAGR综合征LD2A.Y
- Williams-Beuren综合征LD44.70
- Gorham-Stout病FB86.2
- Alagille综合征LB20.0Y
- 耳聋-甲营养不良LD27.0Y
- 常染色体隐性遗传皮肤松弛症，3型LD28.2
- 大头畸形-脱发-皮肤松弛-脊柱侧凸综合征LD28.2
- SCARF综合征LD28.2
- 致命性限制性皮肤病EE6Y
- 脑颅皮肤脂肪过多症EF02.1
- Dahlberg-Borer-Newcomer综合征LD27.0Y
英文词条（38）
- Fraser syndromeLD2H.0
- Waardenburg-Shah syndromeLD2H.3
- Oculocerebrorenal syndrome5C60.0
- Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafnessLD2H.Y
- Bardet-Biedl syndrome5A61.0
- Blepharocheilodontic syndromeLD27.0Y
- Cat-eye syndromeLD41.P
- Cataract - intellectual deficit - hypogonadism5A61.0
- CHARGE syndrome5A61.0
- Coffin-Siris syndromeLD27.0Y
- Dubowitz syndromeLD27.0Y
- Ectodermal dysplasia - ectrodactyly - macular dystrophyLD27.0Y
- Ectrodactyly - ectodermal dysplasia - cleft lip or palateLD27.0Y
- Ectrodactyly - ectodermal dysplasia without cleftingLD27.0Y
- Hirschsprung disease - deafness - polydactylyLD2H.Y
- Limb-mammary syndromeLD27.0Y
- Marshall syndromeLD27.0Y
- MODY 5 syndrome5A13.6
- Nijmegen breakage syndrome-like disorder4A01.31
- Papillorenal syndromeLA13.7Y
- Perrault syndromeLD2H.Y
- Phocomelia - ectrodactyly - deafness - sinus arrhythmiaLD2H.Y
- Shwachman-Diamond syndrome3A70.0
- Smith-Magenis syndromeLD44.H1
- Split hand - split foot - deafnessLD2H.Y
- Triple A syndrome5A74.Y
- Waardenburg syndromeEC23.2Y
- WAGR syndromeLD2A.Y
- Williams-Beuren syndromeLD44.70
- Gorham-Stout diseaseFB86.2
- Alagille syndromeLB20.0Y
- Deafness – onychodystrophyLD27.0Y
- Autosomal recessive cutis laxa, type 3LD28.2
- Macrocephaly – alopecia – cutis laxa – scoliosis syndromeLD28.2
- SCARF syndromeLD28.2
- Lethal restrictive dermopathyEE6Y
- Encephalocraniocutaneous lipomatosisEF02.1
- Dahlberg-Borer-Newcomer syndromeLD27.0Y
子条目 共 9 条
后组配轴 Postcoordination
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。