Ectodermal dysplasia syndrome
MONDO:0019287The 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.
Also known as: ectodermal dysplasia, ectodermal dysplasia (select examples)
45 clinical trials for this condition and its sub-types, 3 tagged with Ectodermal dysplasia syndrome itself.
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Sub-types of Ectodermal dysplasia syndrome
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Dyskeratosis congenita 12 trials
16 sub-types
- DKC1-related disorder 0 trials · 3 incl. sub-types Sub-types →
- Revesz syndrome 2 trials
- Dyskeratosis congenita and related telomere biology disorder 1 trial Sub-types →
- Autosomal recessive dyskeratosis congenita 4 0 trials
- Dyskeratosis congenita, autosomal dominant 1 0 trials
- Dyskeratosis congenita, autosomal dominant 2 0 trials
- Dyskeratosis congenita, autosomal dominant 3 0 trials
- Dyskeratosis congenita, autosomal dominant 4 0 trials
- Dyskeratosis congenita, autosomal dominant 6 0 trials
- Dyskeratosis congenita, autosomal recessive 1 0 trials
- Dyskeratosis congenita, autosomal recessive 2 0 trials
- Dyskeratosis congenita, autosomal recessive 3 0 trials
- Dyskeratosis congenita, autosomal recessive 6 0 trials
- Dyskeratosis congenita, autosomal recessive 7 0 trials
- Dyskeratosis congenita, autosomal recessive 8 0 trials
- Dyskeratosis congenita, digenic 0 trials
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CTSC-related disorder 0 trials · 11 incl. sub-types
3 sub-types
- Periodontitis, aggressive 1 6 trials
- Papillon-Lefevre disease 5 trials
- Haim-Munk syndrome 0 trials
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Cardiofaciocutaneous syndrome 7 trials
4 sub-types
- Cardiofaciocutaneous syndrome 1 1 trial
- Cardiofaciocutaneous syndrome 2 0 trials
- Cardiofaciocutaneous syndrome 3 0 trials
- Cardiofaciocutaneous syndrome 4 0 trials
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Incontinentia pigmenti 3 trials
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Trichothiodystrophy 2 trials
7 sub-types
- Photosensitive trichothiodystrophy 0 trials Sub-types →
- Trichothiodystrophy 4, nonphotosensitive 0 trials
- Trichothiodystrophy 5, nonphotosensitive 0 trials
- Trichothiodystrophy 6, nonphotosensitive 0 trials
- Trichothiodystrophy 7, nonphotosensitive 0 trials
- Trichothiodystrophy 8, nonphotosensitive 0 trials
- Trichothiodystrophy 9, nonphotosensitive 0 trials
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Ectodermal dysplasia WNT10A related 0 trials · 2 incl. sub-types
3 sub-types
- Odonto-onycho-dermal dysplasia 2 trials
- Schöpf-Schulz-Passarge syndrome 0 trials
- Tooth agenesis, selective, 4 0 trials
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Cronkhite-Canada syndrome 1 trial
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Ellis-van Creveld syndrome 1 trial
1 sub-type
- Jeune syndrome situs inversus 0 trials
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Cartilage-hair hypoplasia 1 trial
1 sub-type
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Trichorhinophalangeal syndrome 0 trials · 1 incl. sub-types
2 sub-types
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ADULT syndrome 0 trials
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AREDYLD syndrome 0 trials
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Ackerman syndrome 0 trials
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Barber-Say syndrome 0 trials
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Bartsocas-Papas syndrome 1 0 trials
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Brunoni syndrome 0 trials
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Böök syndrome 0 trials
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CHIME syndrome 0 trials
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Clouston syndrome 0 trials
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Dahlberg-Borer-Newcomer syndrome 0 trials
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Dubowitz syndrome 0 trials
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EEM syndrome 0 trials
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Fontaine progeroid syndrome 0 trials
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Fried's tooth and nail syndrome 0 trials
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GAPO syndrome 0 trials
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Ito hypomelanosis 0 trials
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Johnson neuroectodermal syndrome 0 trials
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KID syndrome 0 trials
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Lelis syndrome 0 trials
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Marshall syndrome 0 trials
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Rapp-Hodgkin syndrome 0 trials
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Schinzel-Giedion syndrome 0 trials
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Stern-Lubinsky-Durrie syndrome 0 trials
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Teebi-Shaltout syndrome 0 trials
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Toriello-Lacassie-Droste syndrome 0 trials
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Acrofacial dysostosis, Weyers type 0 trials
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Alves Castelo dos Santos syndrome 0 trials
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Amelocerebrohypohidrotic syndrome 0 trials
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Ameloonychohypohidrotic syndrome 0 trials
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1 sub-type
- Rosselli-Gulienetti syndrome 0 trials
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Anonychia with flexural pigmentation 0 trials
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Blepharocheilodontic syndrome 0 trials
3 sub-types
- Martinez Monasterio Pinheiro syndrome 0 trials
- Blepharocheilodontic syndrome 1 0 trials
- Blepharocheilodontic syndrome 2 0 trials
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Choroidal atrophy-alopecia syndrome 0 trials
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Cranioectodermal dysplasia 0 trials
7 sub-types
- Cranioectodermal dysplasia 1 0 trials
- Cranioectodermal dysplasia 2 0 trials
- Cranioectodermal dysplasia 3 0 trials
- Cranioectodermal dysplasia 4 0 trials
- Cranioectodermal dysplasia 5 0 trials
- Cranioectodermal dysplasia 6 0 trials
- Short-rib thoracic dysplasia 16 with or without polydactyly 0 trials
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Dermatoosteolysis, Kirghizian type 0 trials
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Dermatopathia pigmentosa reticularis 0 trials
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Dermo-odonto dysplasia 0 trials
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Dermotrichic syndrome 0 trials
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Ectodermal dysplasia Bartalos type 0 trials
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Ectodermal dysplasia blindness 0 trials
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Ectodermal dysplasia margarita type 0 trials
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2 sub-types
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Focal facial dermal dysplasia 0 trials
3 sub-types
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Hypertrichosis lanuginosa congenita 0 trials
2 sub-types
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Jones hersh yusk syndrome 0 trials
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Limb-mammary syndrome 0 trials
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Oculodentodigital dysplasia 0 trials
1 sub-type
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Oculoosteocutaneous syndrome 0 trials
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Oculotrichodysplasia 0 trials
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Odontomicronychial dysplasia 0 trials
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Odontotrichomelic syndrome 0 trials
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Pili torti-onychodysplasia syndrome 0 trials
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4 sub-types
- Ectodermal dysplasia 4, hair/nail type 0 trials
- Ectodermal dysplasia 6, hair/nail type 0 trials
- Ectodermal dysplasia 7, hair/nail type 0 trials
- Ectodermal dysplasia 9, hair/nail type 0 trials
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Scalp-ear-nipple syndrome 0 trials
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Tooth and nail syndrome 0 trials
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Tricho-dento-osseous syndrome 0 trials
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Tricho-retino-dento-digital syndrome 0 trials
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Trichodental syndrome 0 trials
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Trichoodontoonychial dysplasia 0 trials
Most studied deeper sub-types
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Better smiles with 3D printing? new study tests dentures for rare condition
Symptom relief Recruiting nowThis study looks at whether 3D-printed dentures fit better and make patients happier than traditional acrylic dentures in people with ectodermal dysplasia, a rare condition that affects teeth and other body parts. About 11 people aged 10 to 35 who have some remaining teeth will t…
Sponsor: Cairo University • Aim: Symptom relief
Last updated Jun 27, 2026 11:00 UTC
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Scientists hunt for genes behind rare skin condition
Knowledge-focused Recruiting nowThis study aims to find the genes and genetic changes that cause aplasia cutis congenita (ACC), a rare condition where babies are born with missing patches of skin. Researchers will analyze DNA from 600 people with ACC and their family members. The goal is to better understand th…
Sponsor: UConn Health • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:08 UTC
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New study to measure hidden toll of rare skin diseases on patients and families
Knowledge-focused Recruiting nowThis study aims to understand the full burden of 9 rare skin diseases—including physical, emotional, social, and financial challenges—on patients and their families. Researchers will use special questionnaires to track how these conditions affect daily life and care needs. About …
Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:04 UTC