LD90.Y
其他特指的以智力发育障碍为相关临床特征的情况
Other specified conditions with disorders of intellectual development as a relevant clinical feature
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- 3 级
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- 其他特指的以智力发育障碍为相关临床特征的情况
- 以智力发育障碍为相关临床特征的非综合征型情况
- 常染色体显性遗传非综合征型智力缺陷
- 常染色体隐性遗传非综合征型智力缺陷
- X连锁非综合征型智力缺陷
- 非特异性X连锁智力缺陷
- ATR-X相关综合征
- X连锁智力缺陷-面部低张力
- Carpenter-Waziri综合征
- Chudley-Lowry-Hoar综合征
- Holmes-Gang综合征
- Juberg-Marsidi综合征
- Renier-Gabreels-Jasper综合征
- Smith-Fineman-Myers综合征
- X连锁轴索性遗传性运动感觉神经病
- X连锁Charcot-Marie-Tooth病2型
- X连锁腓骨肌萎缩症2型
- X连锁Charcot-Marie-Tooth病3型
- X连锁腓骨肌萎缩症3型
- X连锁Charcot-Marie-Tooth病4型
- X连锁腓骨肌萎缩症4型
- X连锁Charcot-Marie-Tooth病5型
- X连锁腓骨肌萎缩症5型
- Cohen综合征
- 科恩综合征
- FRAXE智力缺陷
- 遗传性过度惊吓反应症
- 先天性僵人综合征
- 遗传性过度惊吓反应症
- 家族性惊跳病
- 僵婴综合征
- 过度惊吓反应症
- Kok疾病
- 婴儿双侧纹状体坏死
- 家族性婴儿双侧纹状体坏死
- 散发性婴儿双侧纹状体坏死
- 婴儿型脊髓小脑共济失调
- IOSCA[婴儿型脊髓小脑共济失调]
- Ohaha[眼肌麻痹-肌张力低下-共济失调-听力减退-手足徐动]综合征
- 眼肌麻痹-肌张力低下-共济失调-听力减退-手足徐动
- 婴儿期发病脑萎缩症
- L1综合征
- Laurence-Moon综合征
- PEHO综合征
- 进行性脑病伴水肿-高度失律脑电图-视神经萎缩综合征
- 进行性脑病伴水肿、高度节律失调和视神经萎缩
- Renpenning综合征
- X连锁智力缺陷，Renpenning型
- Hamel脑-腭-心综合征
- X连锁智力缺陷，Fichera型
- X连锁智力缺陷，Golabi-Ito-Hall型
- X连锁智力缺陷，Porteous型
- X连锁智力缺陷，Sutherland-Haan型
- X连锁智力缺陷，Najm型
- X连锁智力残疾，Najm型
- X连锁痉挛性截瘫2型
- X连锁遗传性脱髓鞘性运动感觉神经病
- CMT X[X连锁Charcot-Marie-Tooth病1型]
- X连锁Charcot-Marie-Tooth病1型
- X连锁腓骨肌萎缩症1型
- 小脑萎缩-共济失调-癫痫发作
- 泛醌缺乏引起的常染色体隐性遗传共济失调
- 辅酶Q10缺乏引起的常染色体隐性遗传共济失调
- 不典型Rett综合征
- De Sanctis-Cacchione综合征
- 着色性干皮病
- SYNGAP1综合征
- 突触Ras-GTP酶激活蛋白1综合征
- 秃发-精神运动性癫痫-牙周脓溢-智力残疾综合征
- Shokeir综合征
英文词条（61）
- Other specified conditions with disorders of intellectual development as a relevant clinical feature
- Non-syndromic conditions with disorders of intellectual development as a relevant clinical feature
- Autosomal dominant non-syndromic intellectual deficit
- Autosomal recessive non-syndromic intellectual deficit
- X-linked non-syndromic intellectual deficit
- Nonspecific X-linked intellectual deficiencies
- ATR-X-related syndromes
- X-linked intellectual deficit - hypotonic face
- Carpenter-Waziri syndrome
- Chudley-Lowry-Hoar syndrome
- Holmes-Gang syndrome
- Juberg-Marsidi syndrome
- Renier-Gabreels-Jasper syndrome
- Smith-Fineman-Myers syndrome
- Axonal hereditary motor and sensory neuropathy, X-linked
- X-linked Charcot-Marie-Tooth disease type 2
- X-linked Charcot-Marie-Tooth disease type 3
- X-linked Charcot-Marie-Tooth disease type 4
- X-linked Charcot-Marie-Tooth disease type 5
- Cohen syndrome
- FRAXE intellectual deficit
- Hereditary hyperekplexia
- Congenital stiff man syndrome
- Familial Startle disease
- Hereditary hyperexplexia
- Hyperekplexia
- Kok disease
- Stiff baby syndrome
- Infantile bilateral striatal necrosis
- Familial infantile bilateral striatal necrosis
- Sporadic infantile bilateral striatal necrosis
- Infantile onset spinocerebellar ataxia
- IOSCA - [infantile onset spinocerebellar ataxia]
- Ohaha - [Ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis] syndrome
- Ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis
- L1 syndrome
- Laurence-Moon syndrome
- PEHO syndrome
- Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy
- Renpenning syndrome
- X-linked intellectual deficit, Renpenning type
- Hamel cerebro-palato-cardiac syndrome
- X-linked intellectual deficit, Fichera type
- X-linked intellectual deficit, Golabi-Ito-Hall type
- X-linked intellectual deficit, Porteous type
- X-linked intellectual deficit, Sutherland-Haan type
- X-linked intellectual deficit, Najm type
- X-linked intellectual disability, Najm type
- X-linked spastic paraplegia type 2
- Demyelinating hereditary motor and sensory neuropathy, X-linked
- CMT X - [X-linked Charcot-Marie-Tooth disease 1]
- X-linked Charcot-Marie-Tooth disease 1
- Cerebellar atrophy - ataxia - seizures
- Autosomal recessive ataxia due to coenzyme Q10 deficiency
- Autosomal recessive ataxia due to ubiquinone deficiency
- Atypical Rett syndrome
- De Sanctis-Cacchione syndrome
- SYNGAP1 syndrome
- synaptic Ras-GTPase-activating protein 1 syndrome
- Alopecia – psychomotor epilepsy – periodontal pyorrhoea – intellectual disability syndrome
- Shokeir syndrome
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。