LD90
以智力发育障碍为相关临床特征的情况
Conditions with disorders of intellectual development as a relevant clinical feature
- 上级条目
- 20 发育异常
- 层级
- 2 级
跨章引用 同一概念在其他章节另有编码
- 莱施-尼汉综合征5C55.01
- 脑积水伴中脑导水管狭窄LA04.0
- 佩-梅病8A44.0
- 遗传性感觉和自主神经病IV 型8C21.2
- 朱伯特综合征LD20.00
- 苯丙酮尿症5C50.0
- 酪氨酸血症2型5C50.12
- 氨甲酰磷酸合成酶缺乏5C50.A1
- 肌肽血症5C50.F1
- 高肌肽病5C50.F2
- 以无脑回畸形为主要特征的综合征LD20.1
- Sjögren-Larsson综合征5C52.03
- 多小脑回LA05.50
- 脑穿通畸形LA05.60
- 丙酮酸脱氢酶复合物缺乏症5C53.02
- 脑-肺-甲状腺综合征CB04.5
- 异染性脑白质营养不良5C56.02
- 神经元蜡样脂褐质贮积症5C56.1
- 黏多糖贮积症2型5C56.31
- 黏多糖贮积症6型5C56.33
- 眼脑肾综合征5C60.0
- CATCH 22表型LD44.N0
- Langer-Giedion综合征LD24.80
- 克里格勒-纳贾综合征5C58.00
- 脆性X染色体LD55
- 色素失禁症LD27.00
- 结节性硬化症LD2D.2
- Noonan综合征LD2F.15
- 先天性风疹综合征KA62.8
- 先天性巨细胞病毒感染KA62.3
- 完全型21三体LD40.0
- 男性Klinefelter综合征，伴多于两条X染色体的LD50.31
- 智力残疾-肠病-耳聋-神经病变-鱼鳞病-角化病综合征LD2H.Y
- 小头畸形-耳聋-智力残疾LD2H.Y
- 精神分裂症-智力残疾-耳聋-视网膜炎LD2H.Y
- 角膜感觉缺失-耳聋-智力残疾LD2H.Y
- 共济失调-耳聋-智力残疾综合征LD2H.Y
- 视网膜色素变性-智力残疾-耳聋-性腺发育不全LD2H.Y
英文词条（38）
- Lesch-Nyhan syndrome5C55.01
- Hydrocephalus with stenosis of the aqueduct of SylviusLA04.0
- Pelizaeus-Merzbacher disease8A44.0
- Hereditary sensory and autonomic neuropathy type IV8C21.2
- Joubert syndromeLD20.00
- Phenylketonuria5C50.0
- Tyrosinaemia type 25C50.12
- Carbamoylphosphate synthetase deficiency5C50.A1
- Carnosinaemia5C50.F1
- Homocarnosinosis5C50.F2
- Syndromes with lissencephaly as a major featureLD20.1
- Sjögren-Larsson syndrome5C52.03
- PolymicrogyriaLA05.50
- PorencephalyLA05.60
- Pyruvate dehydrogenase complex deficiency5C53.02
- Brain-lung-thyroid syndromeCB04.5
- Metachromatic leukodystrophy5C56.02
- Neuronal ceroid lipofuscinosis5C56.1
- Mucopolysaccharidosis type 25C56.31
- Mucopolysaccharidosis type 65C56.33
- Oculocerebrorenal syndrome5C60.0
- CATCH 22 phenotypeLD44.N0
- Langer-Giedion syndromeLD24.80
- Crigler-Najjar syndrome5C58.00
- Fragile X chromosomeLD55
- Incontinentia pigmentiLD27.00
- Tuberous sclerosisLD2D.2
- Noonan syndromeLD2F.15
- Congenital rubella syndromeKA62.8
- Congenital cytomegalovirus infectionKA62.3
- Complete trisomy 21LD40.0
- Klinefelter syndrome, male with more than two X chromosomesLD50.31
- Intellectual disability – enteropathy – deafness – neuropathy – ichthyosis – keratoderma syndromeLD2H.Y
- Microcephaly - deafness - intellectual disabilityLD2H.Y
- Schizophrenia - intellectual disability - deafness - retinitisLD2H.Y
- Corneal anaesthesia - deafness - intellectual disabilityLD2H.Y
- Ataxia - deafness - intellectual disability syndromeLD2H.Y
- Retinitis pigmentosa - intellectual disability - deafness - hypogenitalismLD2H.Y
子条目 共 7 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。