LD27.0Y Other specified ectodermal dysplasia syndromes
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
synonyms
- 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
- Ellis-van Creveld syndrome
- Mesodermic dysplasia
- EVC - [Ellis-van Creveld] syndrome
- 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
- Trichothiodystrophy type G
- ONMR (MIM 258360)
- Itin syndrome
- ONMR syndrome
- 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
- Witkop syndrome (MIM 189500)
- Tooth and nail syndrome
- Amelo-onycho-hypohidrotic syndrome
- Deafness – onychodystrophy
- Deafness – onychodystrophy – osteodystrophy – intellectual deficit
- Deafness – onychodystrophy, autosomal dominant
- DOOR syndrome, autosomal dominant
- Dominant deafness-onychodystrophy
- DDOD syndrome (MIM 124480)
- Deafness – onychodystrophy, autosomal recessive
- DOOR syndrome, autosomal recessive
- DOOR syndrome (MIM 220500)
- 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
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