The term ''ectodermal dysplasia'' defines a heterogeneous group of heritable disorders of the skin and its appendages characterized by the defective development of two or more ectodermal derivatives, including hair, teeth, nails, sweat glands and their modified structures (i.e. ceruminous, mammary and ciliary glands). The spectrum of clinical manifestations is wide and may include additional manifestations from other ectodermal, mesodermal and endodermal structures.
Synonyms: Ectodermal dysplasia
This is just here as a test because I lose it
Term information
database cross reference
- UMLS:C0013575 (E (Exact mapping: the two concepts are equivalent))
- MeSH:D004476 (E (Exact mapping: the two concepts are equivalent))
- MedDRA:10010452 (E (Exact mapping: the two concepts are equivalent))
Term relations
Subclass of:
- Rare developmental defect with skin/mucosae involvement
- Genetic epidermal appendage anomaly
- Epidermal appendage anomaly
- has_age_of_onset some infancy
- has_age_of_onset some neonatal
- present_in some Worldwide and has_point_prevalence_range some 6-9 / 10 000
Related from:
part_of
- Gorlin-Chaudhry-Moss syndrome
- Focal dermal hypoplasia
- Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
- Scalp-ear-nipple syndrome
- Gingival fibromatosis-hypertrichosis syndrome
- Trichodental syndrome
- Tricho-dento-osseous syndrome
- Trichodermodysplasia-dental alterations syndrome
- Trichoodontoonychial dysplasia
- Toriello-Lacassie-Droste syndrome
- GAPO syndrome
- Dermatopathia pigmentosa reticularis
- Hallermann-Streiff syndrome
- Hallermann-Streiff-like syndrome
- Schöpf-Schulz-Passarge syndrome
- CHIME syndrome
- Corneodermatoosseous syndrome
- Skin fragility-woolly hair-palmoplantar keratoderma syndrome
- Arthrogryposis-ectodermal dysplasia syndrome
- Conductive deafness-ptosis-skeletal anomalies syndrome
- Deafness-enamel hypoplasia-nail defects syndrome
- Teebi-Shaltout syndrome
- Cleft lip/palate-ectodermal dysplasia syndrome
- Naegeli-Franceschetti-Jadassohn syndrome
- Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
- Ectodermal dysplasia-syndactyly syndrome
- Ectodermal dysplasia-cutaneous syndactyly syndrome
- Odonto-tricho-ungual-digito-palmar syndrome
- Ectodermal dysplasia with natal teeth, Turnpenny type
- Pure hair and nail ectodermal dysplasia
- Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
- AREDYLD syndrome
- Cerebellar ataxia-ectodermal dysplasia syndrome
- Anonychia with flexural pigmentation
- Böök syndrome
- Tricho-retino-dento-digital syndrome
- Bartsocas-Papas syndrome
- Pyramidal molars-abnormal upper lip syndrome
- Barber-Say syndrome
- Hypodontia-dysplasia of nails syndrome
- Hypertrichosis cubiti
- Hypertrichosis lanuginosa congenita
- Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome
- Hypotrichosis-intellectual disability, Lopes type
- Thumb deformity-alopecia-pigmentation anomaly syndrome
- Johanson-Blizzard syndrome
- Johnson neuroectodermal syndrome
- Amelo-onycho-hypohidrotic syndrome
- Autosomal dominant palmoplantar keratoderma and congenital alopecia
- Alopecia-contractures-dwarfism-intellectual disability syndrome
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
- Lelis syndrome
- Focal facial dermal dysplasia
- Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
- Epidermolysis bullosa simplex due to plakophilin deficiency
- Dermotrichic syndrome
- Fried's tooth and nail syndrome
- Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
- Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
- Hypohidrotic ectodermal dysplasia
- Carvajal syndrome
- Acrofacial dysostosis, Weyers type
- Cronkhite-Canada syndrome
- Dermoodontodysplasia
- Dermatoosteolysis, Kirghizian type
- Hypotrichosis with juvenile macular degeneration
- Pili torti-onychodysplasia syndrome
- Pilodental dysplasia-refractive errors syndrome
- Dahlberg-Borer-Newcomer syndrome
- Papillon-Lefèvre syndrome
- Dyskeratosis congenita
- Schinzel-Giedion syndrome
- Curly hair-acral keratoderma-caries syndrome
- Oculodentodigital dysplasia
- Oculoosteocutaneous syndrome
- Oculotrichodysplasia
- Orofaciodigital syndrome type 1
- CHAND syndrome
- Odonto-onycho-dermal dysplasia
- Odonto-onycho dysplasia-alopecia syndrome
- Odontotrichomelic syndrome
- Cardiofaciocutaneous syndrome
- Cataract-hypertrichosis-intellectual disability syndrome
- Autosomal recessive palmoplantar keratoderma and congenital alopecia
- KID syndrome
- Incontinentia pigmenti
- Cranioectodermal dysplasia
- Chondroectodermal dysplasia with night blindness
- Trichodysplasia-amelogenesis imperfecta syndrome
- Blepharo-cheilo-odontic syndrome
- Cartilage-hair hypoplasia
- Amelocerebrohypohidrotic syndrome
- Hidrotic ectodermal dysplasia
- Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
- Ectodermal dysplasia-sensorineural deafness syndrome
- EEM syndrome
- Hidrotic ectodermal dysplasia, Halal type
- Hidrotic ectodermal dysplasia, Christianson-Fourie type
- Ectodermal dysplasia-blindness syndrome