LD27.0Y
其他特指的外胚层发育不良综合征
Other specified ectodermal dysplasia syndromes
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- 5 级
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- 其他特指的外胚层发育不良综合征
- 无指纹先天性粟丘疹综合征
- Ackerman综合征
- ADULT综合征
- 肢端-皮肤-指（趾）-泪管-牙齿综合征
- 色素异常-先天缺指（缺趾）-先天缺牙
- Propping Zerres综合征
- 釉质-脑-少汗综合征
- Kohlschütter-Tönz综合征
- 癫痫-痴呆-釉质发育不全
- 睑缘粘连-外胚层发育不良-唇裂或腭裂
- 睑缘粘连-外胚层缺陷及唇腭裂综合
- AREDYLD综合征
- 肢端肾缺陷-外胚层发育不良-糖尿病
- Beare-Stevenson回状头皮综合征
- 眼睑-唇-牙综合征
- Book综合征
- 心-面-皮肤综合征
- 小脑共济失调-外胚层发育不良
- 卷发-睑缘粘连-甲发育不良综合征
- CHANDS[卷发-睑缘粘连-甲发育不良综合征]
- Baughman综合征
- 脉络膜萎缩-脱发
- Coffin-Siris综合征
- 传导性耳聋-上睑下垂-骨骼异常
- 挛缩-外胚层发育不良-唇裂或腭裂
- Cote-Katsantoni综合征
- 颅骨外胚层发育不良
- Sensenbrenner综合征
- 森森布伦纳综合征
- Dahlberg-Borer-Newcomer综合征
- 淋巴水肿-甲状旁腺功能减退症
- 皮肤骨溶解，Kirghizian型
- Dubowitz综合征
- 外胚层发育不良-皮纹缺失
- 外胚层发育不良-黑棘皮病
- Lelis综合征
- 外胚层发育不良-关节挛缩-糖尿病
- 外胚层发育不良-盲
- 外胚层发育不良-皮肤性并指综合征
- 外胚层发育不良-先天性缺指-黄斑营养不良
- EEM[外胚层发育不良-先天性缺指-黄斑营养不良]
- 外胚层发育不良-智力缺陷-中枢神经系统畸形
- 外胚层发育不良-感音神经性聋
- 外胚层发育不良-并指综合征
- 外胚层发育不良伴胎生牙，Turnbpenny型
- 外胚层发育不良，纯发-甲型
- 外胚层发育不良，Berlin型
- 先天性缺指-外胚层发育不良-唇裂或腭裂
- EEC[先天性缺指-外胚层发育不良-唇裂或腭裂]
- 先天性缺指-外胚层发育不良，不伴唇腭裂
- 面部外胚层发育不良
- 局灶性颜面真皮发育不良
- 局灶性面部皮肤发育不良
- GAPO综合征
- 生长迟缓-脱发-埋伏牙-视神经萎缩
- 牙龈纤维瘤病-多毛症
- 牙龈纤维瘤病-多毛综合征
- Gorlin-Chaudhry-Moss综合征
- 有汗性外胚层发育不良，Christianson-Fourie型
- 有汗性外胚层发育不良，Halal型
- 肘毛增多症-矮小症
- 甲状旁腺功能减退-聋-肾病
- HDR[甲状旁腺功能减退-聋-肾病]综合征
- Barakat综合征
- 鱼鳞病-脱发-唇外翻-睑外翻-智力缺陷
- Johanson-Blizzard综合征
- Johnson神经外胚层综合征
- 幼年型黄斑变性-少毛症
- 泪管-耳-牙-指综合征
- 泪管-耳-齿-指综合征
- 肢体乳腺综合征
- Marshall综合征
- 马歇尔综合征
- Naegeli-Francechetti-Jadassohn综合征
- 眼-牙-指发育不良
- 眼齿指发育不良
- 眼-骨-皮肤综合征
- 牙-毛发-甲-指（趾）-掌综合征
- 牙-毛发综合征
- OL-EDA-ID综合征
- OLEDAID[无汗性外胚层发育不良-免疫缺陷-石骨症-淋巴水肿]
- 无汗性外胚层发育不良-免疫缺陷-石骨症-淋巴水肿
- 无汗性外胚层发育不良-免疫缺陷-石骨症-淋巴水肿
- 少牙畸形-癌症易感综合征
- 常染色体显性遗传外胚层发育不良-肿瘤综合征
- 毛发牙齿发育不良-屈光不正
- Rapp-Hodgkin综合征
- 头皮-耳-乳头综合征
- Schinzel-Giedion综合征
- 头发稀疏-矮小症-皮肤异常
- Stern-Lubinsky-Durrie综合征
- 牛齿症-缺牙-毛发稀疏
- Toriello-Lacassie-Droste综合征
- 毛发-牙-骨综合征
- 毛发一牙齿一骨综合征
- 毛发-眼-皮肤-椎体综合征
- 毛发-牙-甲发育不良，伴额顶区骨缺乏
- 毛发-牙-甲外胚层发育不良
- 毛发-视网膜-牙-指（趾）综合征
- 毛发-牙综合征
- 毛发真皮发育不良-牙齿改变
- 毛发发育不良-釉质发育不全
- 睫毛粗长症-白内障-遗传性球形红细胞增多症
- 睫毛粗长症-视网膜色素变性-侏儒症
- 干皮病-畸形足-釉质发育缺陷
- Zlotogora-Ogur综合征
- 玛格丽特岛外胚层发育不良
- Rosselli-Gulienetti综合征
- Zlotogora-Martinez综合征
- Zunich-Kaye综合征
- 皮肤-牙齿发育不良
- 皮肤牙齿发育不良
- 眼-毛发发育不良
- 软骨-毛发发育不良
- 毛发-鼻-指（趾）综合征1型和3型
- 软骨外胚层发育不良
- EVC[Ellis-van-Creveld综合征]
- Ellis-van Creveld综合征
- 中胚层发育不良
- 埃利伟氏综合征
- 牙-甲-皮肤发育不良
- OODD（MIM 257980）
- 羊毛状发–少毛症–下唇外翻–突出耳
- Salamon综合征
- 常染色体显性遗传掌跖角化病与先天性脱发
- Stevanovic综合征
- BIDS综合征
- Amish脆发综合征
- 毛发低硫营养不良D型
- 阿米什脆发综合征
- 毛发硫营养障碍D型
- IBIDS综合征
- Tay综合征
- 毛发低硫营养不良E型
- 毛发低硫营养不良伴先天性鱼鳞病
- 毛发硫营养障碍E型
- 毛发硫营养障碍伴先天性鱼鳞病
- Sabinas脆发综合征
- 脆发-精神发育不全
- 毛发低硫营养不良B型
- 毛发硫营养障碍B型
- 萨宾纳斯脆发综合征
- 甲毛发发育不良-中性粒细胞减少综合征
- ONMR综合征
- 毛发低硫营养不良G型
- ONMR（MIM258360）
- Itin综合征
- 毛发硫营养障碍G型
- 甲-毛发育不良
- 常染色体隐性遗传掌跖角化症与先天性脱发
- Wallis综合征
- 脱发-挛缩-侏儒症-智力缺陷
- 白内障-脱发-指端硬化
- 牙-甲发育不良-脱发
- Schöpf-Schulz-Passarge综合征
- 先天性毳毛性多毛症
- 先天性全身多毛症
- 先天性全身性多发症
- 先天性胎毛增多症
- 先天性胎毛性多毛症
- 先天性胎儿性多毛症
- 先天性全身性多毛症
- Ambras综合征
- X连锁显性遗传先天性全身性多毛症
- Macias-Flores综合征
- 耳聋–釉质发育不全-甲缺损
- Heimler综合征
- 感音神经性听力损失伴釉质发育不全和甲缺损
- 感音神经性聋伴釉质发育不全和甲缺损
- 甲缺如伴奇异性屈侧色素沉着
- 甲缺如伴屈侧色素沉着（MIM106750）
- 甲缺如或甲营养不良-发育不全或远端指骨缺失（趾骨缺失）
- Cooks综合征
- 常染色体显性遗传先天性缺牙伴甲发育不良
- Witkop综合征（MIM 189500）
- 牙甲综合征
- 釉质-甲-少汗综合征
- 耳聋-甲营养不良
- 耳聋-甲营养不良-骨营养不良-智力缺陷
- 常染色体显性遗传性耳聋–甲营养不良
- 常染色体显性遗传DOOR综合征
- 显性遗传耳聋-甲营养不良
- DDOD综合征
- 常染色体隐性遗传性耳聋甲营养不良
- 常染色体隐性遗传DOOR综合征
- DOOR综合征（MIM 220500）
- 牙-甲-少汗性外胚层发育不良-中线头皮缺损
- 毛发-牙-指（趾）-皮肤综合征
- 毛发-牙-甲发育不良-显性并指（并趾）畸形
- 毛发扭曲-甲发育不良
- 扭曲发-骨-指(趾)甲营养不良
- 局灶性真皮发育不全
- Goltz综合征
- Goltz-Gorlin综合征
- 家族性单纯性睫毛粗长症
- 家族性单纯性睫毛粗长症
英文词条（175）
- Other specified ectodermal dysplasia syndromes
- Absence of fingerprints-congenital milia syndrome
- Ackerman syndrome
- ADULT syndrome
- Acro-dermato-ungual-lacrimal-tooth syndrome
- Pigment anomaly - ectrodactyly - hypodontia
- Propping Zerres syndrome
- Amelo-cerebro-hypohidrotic syndrome
- Epilepsy - dementia - amelogenesis imperfecta
- Kohlschütter-Tönz syndrome
- Ankyloblepharon - ectodermal defects - cleft lip or palate
- AREDYLD syndrome
- Acrorenal defect - ectodermal dysplasia - diabetes
- Beare-Stevenson cutis gyrata syndrome
- Blepharocheilodontic syndrome
- Book syndrome
- Cardio-facio-cutaneous syndrome
- Cerebellar ataxia - ectodermal dysplasia
- Curly hair – ankyloblepharon – nail dysplasia syndrome
- Baughman syndrome
- CHANDS - [Curly hair - ankyloblepharon - nail dysplasia syndrome]
- Choroidal atrophy - alopecia
- Coffin-Siris syndrome
- Conductive deafness - ptosis - skeletal anomalies
- Contractures - ectodermal dysplasia - cleft lip or palate
- Cote-Katsantoni syndrome
- Cranioectodermal dysplasia
- Sensenbrenner syndrome
- Dahlberg-Borer-Newcomer syndrome
- Lymphoedema - hypoparathyroidism
- Dermatoosteolysis, Kirghizian type
- Dubowitz syndrome
- Ectodermal dysplasia - absent dermatoglyphs
- Ectodermal dysplasia - acanthosis nigricans
- Lelis syndrome
- Ectodermal dysplasia - arthrogryposis - diabetes mellitus
- Ectodermal dysplasia - blindness
- Ectodermal dysplasia - cutaneous syndactyly syndrome
- Ectodermal dysplasia - ectrodactyly - macular dystrophy
- EEM - [Ectodermal dysplasia - ectrodactyly - macular dystrophy] syndrome
- Ectodermal dysplasia - intellectual deficit - central nervous system malformation
- Ectodermal dysplasia - sensorineural deafness
- Ectodermal dysplasia - syndactyly syndrome
- Ectodermal dysplasia with natal teeth, Turnpenny type
- Ectodermal dysplasia, pure hair-nail type
- Ectodermal dysplasia, Berlin type
- Ectrodactyly - ectodermal dysplasia - cleft lip or palate
- EEC - [Ectrodactyly - ectodermal dysplasia - cleft lip or palate] syndrome
- Ectrodactyly - ectodermal dysplasia without clefting
- Facial ectodermal dysplasia
- Focal facial dermal dysplasia
- GAPO syndrome
- Growth delay - alopecia - pseudoanodontia - optic atrophy
- Gingival fibromatosis - hypertrichosis
- Gingival fibromatosis-hypertrichosis syndrome
- Gorlin-Chaudhry-Moss syndrome
- Hidrotic ectodermal dysplasia, Christianson-Fourie type
- Hidrotic ectodermal dysplasia, Halal type
- Hypertrichosis cubiti - short stature
- Hypoparathyroidism - deafness - renal disease
- Barakat syndrome
- HDR - [Hypoparathyroidism - deafness - renal disease] syndrome
- Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit
- Johanson-Blizzard syndrome
- Johnson neuroectodermal syndrome
- Juvenile macular degeneration - hypotrichosis
- Lacrimo-auriculo-dento-digital syndrome
- Limb-mammary syndrome
- Marshall syndrome
- Naegeli-Franceschetti-Jadassohn syndrome
- Oculo-dento-digital dysplasia
- Oculo-osteo-cutaneous syndrome
- Odonto-tricho-ungual-digito-palmar syndrome
- Odontotrichomelic syndrome
- OL-EDA-ID syndrome
- Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphoedema
- OLEDAID - [Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphoedema] syndrome
- Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphoedema
- Oligodontia - cancer predisposition syndrome
- Autosomal dominant ectodermal dysplasia-neoplastic syndrome
- Pilodental dysplasia - refractive errors
- Rapp-Hodgkin syndrome
- Scalp-ear-nipple syndrome
- Schinzel-Giedion syndrome
- Sparse hair - short stature - skin anomalies
- Stern-Lubinsky-Durrie syndrome
- Taurodontia - absent teeth - sparse hair
- Toriello-Lacassie-Droste syndrome
- Tricho-dento-osseous syndrome
- Tricho-oculo-dermo-vertebral syndrome
- Tricho-odonto-onychial dysplasia with bone deficiency in fronto-parietal region
- Tricho-odonto-onychial ectodermal dysplasia
- Tricho-retino-dento-digital syndrome
- Trichodental syndrome
- Trichodermodysplasia - dental alterations
- Trichodysplasia - amelogenesis imperfecta
- Trichomegaly - cataract - hereditary spherocytosis
- Trichomegaly - retina pigmentary degeneration - dwarfism
- Xeroderma - talipes - enamel defects
- Zlotogora-Ogur syndrome
- Margarita island ectodermal dysplasia
- Rosselli-Gulienetti syndrome
- Zlotogora-Martinez syndrome
- Zunich-Kaye syndrome
- Dermo-odontodysplasia
- Dermoodontodysplasia
- Oculotrichodysplasia
- Cartilage-hair hypoplasia
- Trichorhinophalangeal syndrome type 1 and 3
- Chondroectodermal dysplasia
- EVC - [Ellis-van Creveld] syndrome
- Ellis-van Creveld syndrome
- Mesodermic dysplasia
- Odonto-onycho-dermal dysplasia
- OODD (MIM 257980)
- Woolly hair – hypotrichosis – everted lower lip – outstanding ears
- Salamon syndrome
- Autosomal dominant palmoplantar keratoderma and congenital alopecia
- Stevanovic syndrome
- BIDS syndrome
- Amish brittle hair syndrome
- Trichothiodystrophy type D
- IBIDS syndrome
- Tay syndrome
- Trichothiodystrophy type E
- Trichothiodystrophy with congenital ichthyosis
- Sabinas brittle hair syndrome
- Brittle hair - mental deficiency
- Trichothiodystrophy type B
- Onycho-tricho-dysplasia – neutropaenia syndrome
- Itin syndrome
- ONMR (MIM 258360)
- ONMR syndrome
- Trichothiodystrophy type G
- Autosomal recessive palmoplantar keratoderma and congenital alopecia
- Wallis syndrome
- Alopecia - contractures - dwarfism - intellectual deficit
- Cataract - alopecia - sclerodactyly
- Odonto-onycho dysplasia - alopecia
- Schöpf-Schulz-Passarge syndrome
- Hypertrichosis lanuginosa congenita
- Hypertrichosis universalis congenita
- Congenital generalised hypertrichosis
- Ambras syndrome
- X-linked dominant congenital generalised hypertrichosis
- Macias-Flores syndrome
- Deafness – enamel hypoplasia – nail defects
- Heimler syndrome
- Sensorineural hearing loss with enamel hypoplasia and nail defects
- Anonychia with bizarre flexural pigmentation
- Anonychia with flexural pigmentation (MIM 106750)
- Anonychia or onychodystrophy – hypoplasia or absence of distal phalanges
- Cooks syndrome
- Autosomal dominant hypodontia with nail dysplasia
- Tooth and nail syndrome
- Witkop syndrome (MIM 189500)
- Amelo-onycho-hypohidrotic syndrome
- Deafness – onychodystrophy
- Deafness – onychodystrophy – osteodystrophy – intellectual deficit
- Deafness – onychodystrophy, autosomal dominant
- DDOD syndrome
- DOOR syndrome, autosomal dominant
- Dominant deafness-onychodystrophy
- Deafness – onychodystrophy, autosomal recessive
- DOOR syndrome (MIM 220500)
- DOOR syndrome, autosomal recessive
- Odonto-onycho-hypohidrotic dysplasia - midline scalp defects
- Tricho-odonto-onycho-dermal syndrome
- Tricho-odonto-onychodysplasia - dominant syndactyly
- Pili torti - onychodysplasia
- Focal dermal hypoplasia
- Goltz syndrome
- Goltz-Gorlin syndrome
- Familial isolated trichomegaly
- Familial isolated trichomegaly of the eyelashes
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。