Hereditary epidermal appendage anomaly
MONDO:0021026An instance of epidermal appendage anomaly that is caused by a modification of the individual's genome.
Also known as: genetic epidermal appendage anomaly
50 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Dyskeratosis congenita
(12)
Cardiofaciocutaneous syndrome
(6)
Periodontitis, aggressive 1
(6)
Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
(4)
Papillon-Lefevre disease
(4)
Ectodermal dysplasia syndrome
(3)
Hoyeraal-Hreidarsson syndrome
(3)
Incontinentia pigmenti
(3)
Odonto-onycho-dermal dysplasia
(2)
Revesz syndrome
(2)
Trichothiodystrophy
(2)
Cardiofaciocutaneous syndrome 1
(1)
Cartilage-hair hypoplasia
(1)
Cronkhite-Canada syndrome
(1)
Dyskeratosis congenita and related telomere biology disorder
(1)
Ellis-van Creveld syndrome
(1)
Hypohidrotic ectodermal dysplasia
(1)
Trichorhinophalangeal syndrome type II
(1)
Ackerman syndrome
(0)
Acrofacial dysostosis, Weyers type
(0)