Hereditary skin disorder

Part of

Sub-types of Hereditary skin disorder

• Psoriasis 379 trials
  3 sub-types

  • Pustular psoriasis 6 trials · 39 incl. sub-types Sub-types →
  • Guttate psoriasis 2 trials
  • Psoriasis 2 0 trials
• Acne 91 trials
  1 sub-type

  • Adult acne 0 trials
• Hereditary angioedema 58 trials · 60 incl. sub-types
  10 sub-types

  • Hereditary angioedema with C1Inh deficiency 14 trials · 32 incl. sub-types Sub-types →
  • Hereditary angioedema type 3 2 trials
  • Hereditary angioedema with normal C1Inh 2 trials
  • PLG-related hereditary angioedema with normal C1inh 0 trials
  • Angioedema, hereditary, 4 0 trials
  • Angioedema, hereditary, 5 0 trials
  • Angioedema, hereditary, 6 0 trials
  • Angioedema, hereditary, 7 0 trials
  • Angioedema, hereditary, 8 0 trials
  • Hereditary angioedema with normal C1inh not related to F12 or PLG variant 0 trials
• Ectodermal dysplasia syndrome 3 trials · 45 incl. sub-types
  120 sub-types

  • Dyskeratosis congenita 12 trials Sub-types →
  • CTSC-related disorder 0 trials · 11 incl. sub-types Sub-types →
  • Cardiofaciocutaneous syndrome 7 trials Sub-types →
  • Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome 4 trials
  • Incontinentia pigmenti 3 trials
  • Ectodermal dysplasia WNT10A related 0 trials · 2 incl. sub-types Sub-types →
  • Trichothiodystrophy 2 trials Sub-types →
  • Cronkhite-Canada syndrome 1 trial
  • Ellis-van Creveld syndrome 1 trial Sub-types →
  • Cartilage-hair hypoplasia 1 trial Sub-types →
  • Hypohidrotic ectodermal dysplasia 1 trial Sub-types →
  • Trichorhinophalangeal syndrome 0 trials · 1 incl. sub-types Sub-types →
  • ADULT syndrome 0 trials
  • AREDYLD syndrome 0 trials
  • Ackerman syndrome 0 trials
  • Barber-Say syndrome 0 trials
  • Bartsocas-Papas syndrome 1 0 trials
  • Brunoni syndrome 0 trials
  • Böök syndrome 0 trials
  • CHIME syndrome 0 trials
  • Clouston syndrome 0 trials
  • Curly hair - acral keratoderma - caries syndrome 0 trials
  • Dahlberg-Borer-Newcomer syndrome 0 trials
  • Dubowitz syndrome 0 trials
  • EEM syndrome 0 trials
  • Fontaine progeroid syndrome 0 trials
  • Fried's tooth and nail syndrome 0 trials
  • GAPO syndrome 0 trials
  • Ito hypomelanosis 0 trials
  • Johnson neuroectodermal syndrome 0 trials
  • KID syndrome 0 trials Sub-types →
  • Lelis syndrome 0 trials
  • Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome 0 trials
  • Marshall syndrome 0 trials
  • Naegeli-Franceschetti-Jadassohn syndrome 0 trials
  • Rapp-Hodgkin syndrome 0 trials
  • Schinzel-Giedion syndrome 0 trials
  • Stern-Lubinsky-Durrie syndrome 0 trials
  • Teebi-Shaltout syndrome 0 trials
  • Toriello-Lacassie-Droste syndrome 0 trials
  • Acrofacial dysostosis, Weyers type 0 trials
  • Alopecia - contractures - dwarfism - intellectual disability syndrome 0 trials
  • Alves Castelo dos Santos syndrome 0 trials
  • Amelocerebrohypohidrotic syndrome 0 trials
  • Ameloonychohypohidrotic syndrome 0 trials
  • Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 0 trials Sub-types →
  • Anonychia with flexural pigmentation 0 trials
  • Arrhythmogenic cardiomyopathy with wooly hair and keratoderma 0 trials
  • Arthrogryposis-ectodermal dysplasia-other anomalies syndrome 0 trials
  • Autosomal dominant palmoplantar keratoderma and congenital alopecia 0 trials
  • Autosomal dominant trichoodontoonychodysplasia-syndactyly 0 trials
  • Autosomal recessive palmoplantar keratoderma and congenital alopecia 0 trials
  • Blepharocheilodontic syndrome 0 trials Sub-types →
  • Cataract-hypertrichosis-intellectual disability syndrome 0 trials
  • Cerebellar ataxia-ectodermal dysplasia syndrome 0 trials
  • Chondroectodermal dysplasia with night blindness 0 trials
  • Choroidal atrophy-alopecia syndrome 0 trials
  • Circumscribed palmoplantar hypokeratosis 0 trials
  • Cleft lip/palate-ectodermal dysplasia syndrome 0 trials
  • Conductive deafness-ptosis-skeletal anomalies syndrome 0 trials
  • Congenital hypotrichosis with juvenile macular dystrophy 0 trials
  • Contractures-ectodermal dysplasia-cleft lip/palate syndrome 0 trials
  • Cranioectodermal dysplasia 0 trials Sub-types →
  • Dermatoosteolysis, Kirghizian type 0 trials
  • Dermatopathia pigmentosa reticularis 0 trials
  • Dermo-odonto dysplasia 0 trials
  • Dermotrichic syndrome 0 trials
  • Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type 0 trials
  • Ectodermal dysplasia 13, hair/tooth type 0 trials
  • Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis 0 trials
  • Ectodermal dysplasia 15, hypohidrotic/hair type 0 trials
  • Ectodermal dysplasia 17 with or without limb malformations 0 trials
  • Ectodermal dysplasia 5, hair/nail type 0 trials
  • Ectodermal dysplasia Bartalos type 0 trials
  • Ectodermal dysplasia alopecia preaxial polydactyly 0 trials
  • Ectodermal dysplasia arthrogryposis diabetes mellitus 0 trials
  • Ectodermal dysplasia blindness 0 trials
  • Ectodermal dysplasia margarita type 0 trials
  • Ectodermal dysplasia neurosensory deafness 0 trials
  • Ectodermal dysplasia with natal teeth, Turnpenny type 0 trials
  • Ectodermal dysplasia, trichoodontoonychial type 0 trials
  • Ectodermal dysplasia-blindness syndrome 0 trials
  • Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome 0 trials
  • Ectodermal dysplasia-sensorineural deafness syndrome 0 trials
  • Ectodermal dysplasia-syndactyly syndrome 0 trials Sub-types →
  • Epidermolysis bullosa simplex due to plakophilin deficiency 0 trials
  • Focal facial dermal dysplasia 0 trials Sub-types →
  • Gingival fibromatosis-hypertrichosis syndrome 0 trials
  • Hidrotic ectodermal dysplasia, Christianson-Fourie type 0 trials
  • Hidrotic ectodermal dysplasia, Halal type 0 trials
  • Hypertrichosis cubiti-short stature syndrome 0 trials
  • Hypertrichosis lanuginosa congenita 0 trials Sub-types →
  • Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome 0 trials
  • Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome 0 trials
  • Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome 0 trials
  • Jones hersh yusk syndrome 0 trials
  • Limb-mammary syndrome 0 trials
  • Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies 0 trials
  • Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome 0 trials
  • Oculodentodigital dysplasia 0 trials Sub-types →
  • Oculoosteocutaneous syndrome 0 trials
  • Oculotrichodysplasia 0 trials
  • Odonto-onycho dysplasia-alopecia syndrome 0 trials
  • Odonto-tricho-ungual-digito-palmar syndrome 0 trials
  • Odontomicronychial dysplasia 0 trials
  • Odontotrichomelic syndrome 0 trials
  • Pili torti-onychodysplasia syndrome 0 trials
  • Pilodental dysplasia-refractive errors syndrome 0 trials
  • Pure hair and nail ectodermal dysplasia 0 trials Sub-types →
  • Scalp-ear-nipple syndrome 0 trials
  • Taurodontia-absent teeth-sparse hair syndrome 0 trials
  • Tooth and nail syndrome 0 trials
  • Tricho-dento-osseous syndrome 0 trials
  • Tricho-oculo-dermo-vertebral syndrome 0 trials
  • Tricho-retino-dento-digital syndrome 0 trials
  • Trichodental syndrome 0 trials
  • Trichodermodysplasia-dental alterations syndrome 0 trials
  • Trichodysplasia-amelogenesis imperfecta syndrome 0 trials
  • Trichomegaly-retina pigmentary degeneration-dwarfism syndrome 0 trials
  • Trichoodontoonychial dysplasia 0 trials
• CHILD syndrome 37 trials
• Inherited epidermolysis bullosa 5 trials · 37 incl. sub-types
  4 sub-types

  • Epidermolysis bullosa dystrophica 23 trials · 30 incl. sub-types Sub-types →
  • Junctional epidermolysis bullosa 6 trials · 8 incl. sub-types Sub-types →
  • Epidermolysis bullosa simplex 5 trials Sub-types →
  • Kindler syndrome 0 trials Sub-types →
• Inherited ichthyosis 6 trials · 32 incl. sub-types
  13 sub-types

  • Netherton syndrome 15 trials
  • Autosomal recessive congenital ichthyosis 2 trials · 10 incl. sub-types Sub-types →
  • Keratinopathic ichthyosis 0 trials · 7 incl. sub-types Sub-types →
  • Ichthyosis vulgaris 3 trials Sub-types →
  • Recessive X-linked ichthyosis 2 trials Sub-types →
  • Peeling skin syndrome 1 trial Sub-types →
  • IFAP syndrome 0 trials Sub-types →
  • Congenital cataract-ichthyosis syndrome 0 trials
  • Ichthyosis hystrix 0 trials Sub-types →
  • Ichthyosis linearis circumflexa 0 trials
  • Ichthyosis with erythrokeratoderma 0 trials
  • Ichthyosis-oral and digital anomalies syndrome 0 trials
  • Neonatal ichthyosis-sclerosing cholangitis syndrome 0 trials
• Hereditary photodermatosis 0 trials · 31 incl. sub-types
  6 sub-types

  • Inherited porphyria 0 trials · 24 incl. sub-types Sub-types →
  • Xeroderma pigmentosum 4 trials · 6 incl. sub-types Sub-types →
  • Xeroderma pigmentosum-Cockayne syndrome complex 1 trial · 2 incl. sub-types Sub-types →
  • Rothmund-Thomson syndrome 1 trial Sub-types →
  • Bloom syndrome 0 trials
  • UV-sensitive syndrome 0 trials Sub-types →
• Lichen sclerosus et atrophicus 10 trials · 20 incl. sub-types
  1 sub-type

  • Vulvar lichen sclerosus 15 trials
• Hereditary lipodystrophy 2 trials · 17 incl. sub-types
  11 sub-types

  • Familial partial lipodystrophy 13 trials · 14 incl. sub-types Sub-types →
  • Congenital generalized lipodystrophy 2 trials · 3 incl. sub-types Sub-types →
  • Berardinelli-Seip congenital lipodystrophy 0 trials · 1 incl. sub-types Sub-types →
  • Keppen-Lubinsky syndrome 0 trials
  • SHORT syndrome 0 trials
  • Wiedemann-Rautenstrauch syndrome 0 trials
  • Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy 0 trials
  • Lipodystrophy due to peptidic growth factors deficiency 0 trials
  • Lipodystrophy-intellectual disability-deafness syndrome 0 trials
  • Mandibuloacral dysplasia 0 trials Sub-types →
  • Severe neurodegenerative syndrome with lipodystrophy 0 trials
• Hereditary palmoplantar keratoderma 0 trials · 13 incl. sub-types
  8 sub-types

  • Diffuse palmoplantar keratoderma 0 trials · 12 incl. sub-types Sub-types →
  • Olmsted syndrome 1 trial Sub-types →
  • Focal palmoplantar keratoderma 0 trials · 1 incl. sub-types Sub-types →
  • Palmoplantar keratoderma, epidermolytic 0 trials · 1 incl. sub-types Sub-types →
  • Alopecia congenita keratosis palmoplantaris 0 trials
  • Palmoplantar keratoderma i, striate, focal, or diffuse 0 trials
  • Palmoplantar keratoderma, nonepidermolytic, focal or diffuse 0 trials
  • Punctate palmoplantar keratoderma 0 trials Sub-types →
• Familial multiple nevi flammei 12 trials
• Syndromic oculocutaneous albinism 0 trials · 12 incl. sub-types
  4 sub-types

  • Chediak-Higashi syndrome 9 trials
  • Hermansky-Pudlak syndrome 4 trials Sub-types →
  • Griscelli syndrome 2 trials · 3 incl. sub-types Sub-types →
  • Oculocerebral hypopigmentation syndrome, Cross type 0 trials
• Cowden disease 11 trials
  8 sub-types

  • Cowden syndrome 1 1 trial
  • Cowden syndrome 2 0 trials
  • Cowden syndrome 3 0 trials
  • Cowden syndrome 4 0 trials
  • Cowden syndrome 5 0 trials
  • Cowden syndrome 6 0 trials
  • Cowden syndrome 7 0 trials
  • Sacral hemangiomas multiple congenital abnormalities 0 trials
• 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
  5 sub-types

  • Eyelid seborrheic keratosis 0 trials
  • Inflamed seborrheic keratosis 0 trials
  • Inverted follicular keratosis 0 trials Sub-types →
  • Melanoacanthoma 0 trials
  • Vulvar seborrheic keratosis 0 trials Sub-types →
• Alopecia, isolated 0 trials · 6 incl. sub-types
  8 sub-types

  • Alopecia universalis congenita 6 trials
  • Alopecia areata 1 0 trials
  • Alopecia areata 2 0 trials
  • Alopecia, androgenetic, 1 0 trials
  • Alopecia, androgenetic, 2 0 trials
  • Alopecia, androgenetic, 3 0 trials
  • Alopecia, congenital 0 trials
  • Familial focal alopecia 0 trials
• CLOVES syndrome 5 trials
• Legius syndrome 5 trials
• Reticulate pigment disorder 0 trials · 5 incl. sub-types
  3 sub-types

  • Dowling-Degos disease 0 trials · 4 incl. sub-types Sub-types →
  • Dyschromatosis symmetrica hereditaria 1 trial
  • Reticulate acropigmentation of Kitamura 0 trials
• Chronic mucocutaneous candidiasis 4 trials
  12 sub-types

  • Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome 0 trials
  • Candidiasis, familial, 1 0 trials
  • Candidiasis, familial, 3 0 trials
  • Candidiasis, familial, 4 0 trials
  • Candidiasis, familial, 6 0 trials
  • Candidiasis, familial, 8 0 trials
  • Candidiasis, familial, 9 0 trials
  • Chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation 0 trials
  • Chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation 0 trials
  • Chronic mucocutaneous candidiasis due to lymphokine deficiency 0 trials
  • Chronic mucocutaneous candidiasis due to monocyte chemotactic disorder 0 trials
  • Immunodeficiency 51 0 trials
• Lamellar ichthyosis 4 trials
  6 sub-types

  • Autosomal recessive congenital ichthyosis 6 1 trial
  • Autosomal recessive congenital ichthyosis 3 0 trials
  • Autosomal recessive congenital ichthyosis 4A 0 trials Sub-types →
  • Autosomal recessive congenital ichthyosis 5 0 trials
  • Autosomal recessive congenital ichthyosis 8 0 trials
  • Ichthyosis, lamellar, autosomal dominant 0 trials
• Oculocutaneous albinism 4 trials
  9 sub-types

  • Oculocutaneous albinism type 1 0 trials · 1 incl. sub-types Sub-types →
  • Autosomal dominant oculocutaneous albinism 0 trials
  • Oculocutaneous albinism type 2 0 trials
  • Oculocutaneous albinism type 3 0 trials
  • Oculocutaneous albinism type 4 0 trials
  • Oculocutaneous albinism type 5 0 trials
  • Oculocutaneous albinism type 6 0 trials
  • Oculocutaneous albinism type 7 0 trials
  • Oculocutaneous albinism type 8 0 trials
• Piebaldism 4 trials
• Hailey-Hailey disease 3 trials
• Aplasia cutis congenita 3 trials
  3 sub-types

  • Aplasia cutis autosomal recessive 0 trials
  • Aplasia cutis congenita dominant 0 trials
  • Aplasia cutis-myopia syndrome 0 trials
• Hereditary mucosal leukokeratosis 3 trials
  2 sub-types

  • White sponge nevus 1 0 trials
  • White sponge nevus 2 0 trials
• Schwannomatosis 3 trials
  4 sub-types

  • 22q-related schwannomatosis 0 trials
  • LZTR1-related schwannomatosis 0 trials
  • SMARCB1-related schwannomatosis 0 trials
  • Neurofibromatosis, type III, mixed central and peripheral 0 trials
• 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
  2 sub-types

  • Chilblain lupus 1 0 trials
  • Chilblain lupus 2 0 trials
• Keratosis pilaris atrophicans 2 trials
  4 sub-types

  • Atrophoderma vermiculata 0 trials
  • Keratosis follicularis spinulosa decalvans 0 trials Sub-types →
  • Keratosis pilaris atrophicans faciei 0 trials
  • Ulerythema ophryogenesis 0 trials
• Stiff skin syndrome 2 trials
  1 sub-type

  • Fascial dystrophy, congenital 0 trials
• Sweet syndrome 2 trials
• Tietz syndrome 1 trial
• X-linked chondrodysplasia punctata 2 1 trial
• Acrokeratosis verruciformis 1 trial
• Dyschromatosis universalis hereditaria 1 trial
  3 sub-types

  • Dyschromatosis universalis hereditaria 1 0 trials
  • Dyschromatosis universalis hereditaria 2 0 trials
  • Dyschromatosis universalis hereditaria 3 0 trials
• Familial primary localized cutaneous amyloidosis 1 trial
  3 sub-types

  • Amyloidosis, primary localized cutaneous, 1 0 trials
  • Amyloidosis, primary localized cutaneous, 2 0 trials
  • Amyloidosis, primary localized cutaneous, 3 0 trials
• Linear nevus sebaceous syndrome 1 trial
• Neurocutaneous melanocytosis 1 trial
• Nevus, epidermal 1 trial
  1 sub-type

  • Wooly hair nevus 0 trials
• Urticaria, aquagenic 1 trial
• Urticaria, familial localized heat 1 trial
• Becker nevus syndrome 0 trials
  1 sub-type

  • Linear and whorled nevoid hypermelanosis 0 trials
• 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
  1 sub-type

  • Wrinkly skin syndrome 0 trials
• 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
  1 sub-type

  • Epidermodysplasia verruciformis, X-linked 0 trials
• Familial acanthosis nigricans 0 trials
• Familial acne inversa 0 trials
  3 sub-types

  • Acne inversa, familial, 1 0 trials
  • Acne inversa, familial, 2 0 trials
  • Acne inversa, familial, 3 0 trials
• 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
  1 sub-type

  • Familial progressive hyper- and hypopigmentation 0 trials
• 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
  3 sub-types

  • Linear skin defects with multiple congenital anomalies 1 0 trials
  • Linear skin defects with multiple congenital anomalies 2 0 trials
  • Linear skin defects with multiple congenital anomalies 3 0 trials
• Lipoid proteinosis 0 trials
• Monilethrix 0 trials
  3 sub-types

  • Monilethrix-1 0 trials
  • Monilethrix-2 0 trials
  • Monilethrix-3 0 trials
• Multiple benign circumferential skin creases on limbs 1 0 trials
• Neonatal inflammatory skin and bowel disease 0 trials
  2 sub-types

  • Inflammatory skin and bowel disease, neonatal, 1 0 trials
  • Inflammatory skin and bowel disease, neonatal, 2 0 trials
• 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
  4 sub-types

  • Disseminated superficial actinic porokeratosis 0 trials Sub-types →
  • Linear porokeratosis 0 trials
  • Porokeratosis of Mibelli 0 trials Sub-types →
  • Porokeratosis plantaris palmaris et disseminata 0 trials
• 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