Watch the Webinar

×

Coding experts Alicia and Laureen from CCO review the new 2025 ICD-10-CM code changes.

View Webinar Recording

close

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

Thank you for choosing Find-A-Code, please Sign In to remove ads.