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Up to: Hereditary disease · Skin disorder

Hereditary skin disorder

An instance of skin disease that is caused by a modification of the individual's genome.

7 trials tagged with this condition →

Psoriasis 379 trials Sub-types →
Acne 91 trials Sub-types →
Hereditary angioedema 58 trials · 60 incl. sub-types Sub-types →
Ectodermal dysplasia syndrome 3 trials · 45 incl. sub-types Sub-types →
CHILD syndrome 37 trials
Inherited epidermolysis bullosa 5 trials · 37 incl. sub-types Sub-types →
Inherited ichthyosis 6 trials · 32 incl. sub-types Sub-types →
Hereditary photodermatosis 0 trials · 31 incl. sub-types Sub-types →
Lichen sclerosus et atrophicus 10 trials · 20 incl. sub-types Sub-types →
Hereditary lipodystrophy 2 trials · 17 incl. sub-types Sub-types →
Hereditary palmoplantar keratoderma 0 trials · 13 incl. sub-types Sub-types →
Familial multiple nevi flammei 12 trials
Syndromic oculocutaneous albinism 0 trials · 12 incl. sub-types Sub-types →
Cowden disease 11 trials Sub-types →
Familial pityriasis rubra pilaris 10 trials
Lentigo 8 trials
Subcutaneous panniculitis-like T-cell lymphoma 8 trials
Large congenital melanocytic nevus 7 trials
Neutrophil actin dysfunction 6 trials
Seborrheic keratosis 6 trials Sub-types →
Alopecia, isolated 0 trials · 6 incl. sub-types Sub-types →
CLOVES syndrome 5 trials
Legius syndrome 5 trials
Reticulate pigment disorder 0 trials · 5 incl. sub-types Sub-types →
Chronic mucocutaneous candidiasis 4 trials Sub-types →
Lamellar ichthyosis 4 trials Sub-types →
Oculocutaneous albinism 4 trials Sub-types →
Piebaldism 4 trials
Hailey-Hailey disease 3 trials
Aplasia cutis congenita 3 trials Sub-types →
Hereditary mucosal leukokeratosis 3 trials Sub-types →
Schwannomatosis 3 trials Sub-types →
Maffucci syndrome 2 trials
Sneddon syndrome 2 trials
Autosomal dominant vibratory urticaria 2 trials
Blue rubber bleb nevus 2 trials
Familial chilblain lupus 2 trials Sub-types →
Keratosis pilaris atrophicans 2 trials Sub-types →
Stiff skin syndrome 2 trials Sub-types →
Sweet syndrome 2 trials
Tietz syndrome 1 trial
X-linked chondrodysplasia punctata 2 1 trial
Acrokeratosis verruciformis 1 trial
Dyschromatosis universalis hereditaria 1 trial Sub-types →
Familial primary localized cutaneous amyloidosis 1 trial Sub-types →
Linear nevus sebaceous syndrome 1 trial
Neurocutaneous melanocytosis 1 trial
Nevus, epidermal 1 trial Sub-types →
Urticaria, aquagenic 1 trial
Urticaria, familial localized heat 1 trial
Becker nevus syndrome 0 trials Sub-types →
Cobb syndrome 0 trials
DK1-congenital disorder of glycosylation 0 trials
Darier disease 0 trials
H syndrome 0 trials
MEDNIK syndrome 0 trials
PENS syndrome 0 trials
VPS13A-related neurodegenerative disease 0 trials
X-linked reticulate pigmentary disorder 0 trials
Absence of fingerprints-congenital milia syndrome 0 trials
Acrogeria 0 trials
Albinism-hearing loss syndrome 0 trials
Anhidrosis, familial generalized, with abnormal or absent sweat glands 0 trials
Autosomal recessive cutis laxa type 2A 0 trials Sub-types →
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency 0 trials
Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis 0 trials
Combined immunodeficiency with skin granulomas 0 trials
Deafness, congenital, with total albinism 0 trials
Dermatitis herpetiformis, familial 0 trials
Dermatosis papulosa nigra 0 trials
Encephalocraniocutaneous lipomatosis 0 trials
Epidermodysplasia verruciformis 0 trials Sub-types →
Familial acanthosis nigricans 0 trials
Familial acne inversa 0 trials Sub-types →
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome 0 trials
Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome 0 trials
Familial keratoacanthoma 0 trials
Familial multiple discoid fibromas 0 trials
Familial multiple fibrofolliculoma 0 trials
Generalized basaloid follicular hamartoma syndrome 0 trials
Hereditary mucoepithelial dysplasia 0 trials
Hereditary papulotranslucent acrokeratoderma 0 trials
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement 0 trials
Hydroa vacciniforme, familial 0 trials
Hyperkeratosis-hyperpigmentation syndrome 0 trials
Hyperpigmentation with or without hypopigmentation, familial progressive 0 trials Sub-types →
Inflammatory poikiloderma with hair abnormalities and acral keratoses 0 trials
Infundibulocystic basal cell carcinoma 0 trials
Isolated anhidrosis with normal sweat glands 0 trials
Isolated congenital adermatoglyphia 0 trials
Isolated hyperchlorhidrosis 0 trials
Juvenile hyaline fibromatosis 0 trials
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome 0 trials
Lichen planus, familial 0 trials
Linear skin defects with multiple congenital anomalies 0 trials Sub-types →
Lipoid proteinosis 0 trials
Monilethrix 0 trials Sub-types →
Multiple benign circumferential skin creases on limbs 1 0 trials
Neonatal inflammatory skin and bowel disease 0 trials Sub-types →
Nevus comedonicus syndrome 0 trials
Osteopathia striata-pigmentary dermopathy-white forelock syndrome 0 trials
Phakomatosis pigmentokeratotica 0 trials
Pilomatrixoma 0 trials
Poikiloderma with neutropenia 0 trials
Porokeratosis 0 trials Sub-types →
Progressive osseous heteroplasia 0 trials
Scalp defects-postaxial polydactyly syndrome 0 trials
Sebocystomatosis 0 trials
Seborrhea-like dermatitis with psoriasiform elements 0 trials
Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome 0 trials
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome 0 trials
Skin creases, congenital symmetric circumferential, 2 0 trials
Spinocerebellar ataxia type 34 0 trials
Vasculitis, lymphocytic, nodular 0 trials