LD27.4
影响甲的遗传综合征
Genetic syndromes affecting nails
- 层级
- 4 级
跨章引用 同一概念在其他章节另有编码
- Wilson病5C64.00
- 指甲-髌骨综合征LD24.J0
- 出汗性外胚层发育不良，Clouston型LD27.03
- 严重T细胞免疫缺陷-先天性秃发-甲营养不良4A01.1Y
- 牙-甲-皮肤发育不良LD27.0Y
- 甲毛发发育不良-中性粒细胞减少综合征LD27.0Y
- 指节垫–白甲–感音神经性聋LD2H.Y
- 耳聋–釉质发育不全-甲缺损LD27.0Y
- 甲缺如伴奇异性屈侧色素沉着LD27.0Y
- 甲缺如或甲营养不良-发育不全或远端指骨缺失（趾骨缺失）LD27.0Y
- 常染色体显性遗传先天性缺牙伴甲发育不良LD27.0Y
- 釉质-甲-少汗综合征LD27.0Y
- 耳聋-甲营养不良LD27.0Y
- 牙-甲-少汗性外胚层发育不良-中线头皮缺损LD27.0Y
- 毛发-牙-指（趾）-皮肤综合征LD27.0Y
- 毛发-牙-甲发育不良-显性并指（并趾）畸形LD27.0Y
- 毛发扭曲-甲发育不良LD27.0Y
- 先天性角化不良3A70.0
- 原发性肥大性骨关节病FB86.10
英文词条（19）
- Wilson disease5C64.00
- Nail-patella syndromeLD24.J0
- Hidrotic ectodermal dysplasia, Clouston typeLD27.03
- Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy4A01.1Y
- Odonto-onycho-dermal dysplasiaLD27.0Y
- Onycho-tricho-dysplasia – neutropaenia syndromeLD27.0Y
- Knuckle pads – leukonychia – sensorineural deafnessLD2H.Y
- Deafness – enamel hypoplasia – nail defectsLD27.0Y
- Anonychia with bizarre flexural pigmentationLD27.0Y
- Anonychia or onychodystrophy – hypoplasia or absence of distal phalangesLD27.0Y
- Autosomal dominant hypodontia with nail dysplasiaLD27.0Y
- Amelo-onycho-hypohidrotic syndromeLD27.0Y
- Deafness – onychodystrophyLD27.0Y
- Odonto-onycho-hypohidrotic dysplasia - midline scalp defectsLD27.0Y
- Tricho-odonto-onycho-dermal syndromeLD27.0Y
- Tricho-odonto-onychodysplasia - dominant syndactylyLD27.0Y
- Pili torti - onychodysplasiaLD27.0Y
- Dyskeratosis congenita3A70.0
- Primary hypertrophic osteoarthropathyFB86.10
索引词 可用于检索该条目的同义词与别名
- 影响甲的遗传综合征
- 耳-甲-腓骨综合征
- 眼-耳-鼻畸形伴骨-甲发育不良（MIM 259780）
- 先天性示指甲发育不良
- COIF[先天性示指甲发育不良]综合征
- Kikuchi综合征
- 分类于他处的大疱性表皮松解症引起的甲营养不良
- 其他特指的遗传病引起的甲受累
英文词条（8）
- Genetic syndromes affecting nails
- Oto-onycho-peroneal syndrome
- Oculo-oto-nasal malformations with osteo-onychodysplasia (MIM 259780)
- Congenital onychodysplasia of the index fingers
- COIF - [Congenital onychodysplasia of the index fingers] syndrome
- Kikuchi syndrome
- Nail dystrophy resulting from epidermolysis bullosa classified elsewhere
- Nail involvement in other specified genetic disease
后组配轴 Postcoordination
后组配是在主干编码之后追加的可选扩展轴（如侧别、具体解剖部位、严重程度），用于把「部位 + 侧别 + 病程」等细节一次表达完整。只有标注「必填」的轴在组合编码时必须给出，其余可留空。
- 侧别laterality可选