SE-ATLAS

Cataract-hypertrichosis-intellectual disability syndrome Hypertrichosis-acromegaloid facial appearance syndrome Trichorhinophalangeal syndrome Epidermolysis bullosa simplex due to exophilin 5 deficiency Congenital cataract-ichthyosis syndrome Congenital ichthyosiform erythroderma Marshall syndrome Cranioectodermal dysplasia Autosomal dominant generalized epidermolysis bullosa simplex, severe form ANE syndrome Ellis Van Creveld syndrome Keratoderma hereditarium mutilans with ichthyosis Familial isolated trichomegaly Teebi-Shaltout syndrome Alopecia totalis Epidermolysis bullosa simplex with mottled pigmentation Localized epidermolysis bullosa simplex Alopecia universalis Dermatoosteolysis, Kirghizian type Acral self-healing collodion baby Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form Trichodysplasia-amelogenesis imperfecta syndrome GAPO syndrome Intermediate generalized junctional epidermolysis bullosa Ichthyosis-hypotrichosis syndrome PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement Orofaciodigital syndrome type 1 Localized junctional epidermolysis bullosa Severe generalized junctional epidermolysis bullosa Dermoodontodysplasia ADULT syndrome Self-improving collodion baby Sparse hair-short stature-skin anomalies syndrome Junctional epidermolysis bullosa with pyloric atresia Pili torti Late-onset junctional epidermolysis bullosa Pili torti-onychodysplasia syndrome Ito hypomelanosis Junctional epidermolysis bullosa inversa Pili torti-developmental delay-neurological abnormalities syndrome Focal facial dermal dysplasia type I Monilethrix Pilodental dysplasia-refractive errors syndrome Recessive dystrophic epidermolysis bullosa inversa Acral peeling skin syndrome Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form Dystrophic epidermolysis bullosa Self-improving dystrophic epidermolysis bullosa Localized dystrophic epidermolysis bullosa, pretibial form Epidermolysis bullosa simplex Loose anagen syndrome Exfoliative ichthyosis Junctional epidermolysis bullosa Ringed hair disease Ectodermal dysplasia-blindness syndrome Woolly hair Focal facial dermal dysplasia type III Focal facial dermal dysplasia Böök syndrome Marie Unna hereditary hypotrichosis Hidrotic ectodermal dysplasia, Christianson-Fourie type Woolly hair nevus Osteosclerosis-ichthyosis-premature ovarian failure syndrome Hidrotic ectodermal dysplasia, Halal type Tricho-retino-dento-digital syndrome Generalized peeling skin syndrome Amelocerebrohypohidrotic syndrome Autosomal dominant hypohidrotic ectodermal dysplasia Hypertrichosis cubiti Pili bifurcati Acquired hypertrichosis lanuginosa Cartilage-hair hypoplasia Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome Autosomal dominant epidermolytic ichthyosis Basal epidermolysis bullosa simplex Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Hypertrichosis lanuginosa congenita Peeling skin syndrome type A Dermatopathia pigmentosa reticularis Lamellar ichthyosis Suprabasal epidermolysis bullosa simplex Annular epidermolytic ichthyosis AREDYLD syndrome Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Ectodermal dysplasia-skin fragility syndrome Peeling skin syndrome type B Focal facial dermal dysplasia type II Kindler epidermolysis bullosa Lacrimoauriculodentodigital syndrome Erythrokeratodermia variabilis Hair defect-photosensitivity-intellectual disability syndrome X-linked hypohidrotic ectodermal dysplasia Ectodermal dysplasia, trichoodontoonychial type Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome Hypodontia-dysplasia of nails syndrome Focal dermal hypoplasia Lelis syndrome Uncombable hair syndrome Peeling skin syndrome type C Localized dystrophic epidermolysis bullosa, acral form Bathing suit ichthyosis Harlequin ichthyosis Gorlin-Chaudhry-Moss syndrome Alopecia-contractures-dwarfism-intellectual disability syndrome Localized dystrophic epidermolysis bullosa, nails only Alopecia antibody deficiency Recessive X-linked ichthyosis Hidrotic ectodermal dysplasia Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Incontinentia pigmenti Autosomal dominant palmoplantar keratoderma and congenital alopecia Epidermolysis bullosa simplex with circinate migratory erythema Corneodermatoosseous syndrome Hypohidrotic ectodermal dysplasia Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Trichorhinophalangeal syndrome type 1 Hallermann-Streiff syndrome Dahlberg-Borer-Newcomer syndrome Curly hair-acral keratoderma-caries syndrome Epidermolysis bullosa simplex with pyloric atresia CHIME syndrome Crandall syndrome Focal facial dermal dysplasia type IV Hypohidrotic ectodermal dysplasia with immunodeficiency Ectodermal dysplasia with natal teeth, Turnpenny type Frontonasal dysplasia-alopecia-genital anomalies syndrome Congenital generalized hypertrichosis, Ambras type Choroidal atrophy-alopecia syndrome Odonto-tricho-ungual-digito-palmar syndrome Limb-mammary syndrome Schöpf-Schulz-Passarge syndrome Pure hair and nail ectodermal dysplasia Hypotrichosis with juvenile macular degeneration Amelo-onycho-hypohidrotic syndrome CEDNIK syndrome Quinquaud folliculitis decalvans Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Naegeli-Franceschetti-Jadassohn syndrome Cleft lip/palate-ectodermal dysplasia syndrome Atrichia with papular lesions Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Trichodental syndrome Hypotrichosis simplex of the scalp Tricho-dento-osseous syndrome Trichodermodysplasia-dental alterations syndrome Tricho-oculo-dermo-vertebral syndrome Trichoodontoonychial dysplasia Cerebellar ataxia-ectodermal dysplasia syndrome Deafness-enamel hypoplasia-nail defects syndrome Autosomal dominant trichoodontoonychodysplasia-syndactyly Trichothiodystrophy Ichthyosis-cheek-eyebrow syndrome Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Trichodysplasia-xeroderma syndrome Blepharo-cheilo-odontic syndrome Laryngo-onycho-cutaneous syndrome Netherton syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Ichthyosis-oral and digital anomalies syndrome Ichthyosis follicularis-alopecia-photophobia syndrome Autosomal recessive generalized epidermolysis bullosa simplex Congenital reticular ichthyosiform erythroderma Trichorhinophalangeal syndrome type 2 Hypotrichosis-deafness syndrome Junctional epidermolysis bullosa, non-Herlitz type Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Deafness-onychodystrophy syndrome Epidermolysis bullosa simplex superficialis Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form Graham Little-Piccardi-Lassueur syndrome Dystrophic epidermolysis bullosa pruriginosa Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome Centripetalis recessive dystrophic epidermolysis bullosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Dubowitz syndrome Conductive deafness-ptosis-skeletal anomalies syndrome Ichthyosis-prematurity syndrome Pyramidal molars-abnormal upper lip syndrome Fried's tooth and nail syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Noonan syndrome-like disorder with loose anagen hair Ectodermal dysplasia-sensorineural deafness syndrome Pili gemini Autosomal recessive hypohidrotic ectodermal dysplasia Ichthyosis Anonychia with flexural pigmentation Cardiofaciocutaneous syndrome Autosomal dominant generalized dystrophic epidermolysis bullosa Lichen planopilaris Cleft lip/palate-ectodermal dysplasia syndrome Schinzel-Giedion syndrome Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome X-linked congenital generalized hypertrichosis Gingival fibromatosis-hypertrichosis syndrome Inherited epidermolysis bullosa Contractures-ectodermal dysplasia-cleft lip/palate syndrome Ichthyosis hystrix gravior Autosomal ichthyosis syndrome with prominent hair abnormalities EEM syndrome Syndromic hair shaft abnormality Ichthyosis hystrix of Curth-Macklin Oculotrichodysplasia Scalp-ear-nipple syndrome Rare disorder with hypertrichosis Syndromic recessive X-linked ichthyosis Isolated hair shaft abnormality Björnstad syndrome Autosomal dominant deafness-onychodystrophy syndrome Oculodentodigital dysplasia Alopecia Frontal fibrosing alopecia DOORS syndrome Chondroectodermal dysplasia with night blindness Epidermolysis bullosa simplex with muscular dystrophy Alopecia-intellectual disability syndrome Isolated anterior cervical hypertrichosis EEC syndrome Lethal acantholytic erosive disorder Inherited ichthyosis syndromic form Oculoosteocutaneous syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Toriello-Lacassie-Droste syndrome X-linked dominant chondrodysplasia punctata Dermotrichic syndrome Cronkhite-Canada syndrome Superficial epidermolytic ichthyosis Cooks syndrome KID syndrome Ectodermal dysplasia syndrome Pseudopelade of Brocq Odonto-onycho-dermal dysplasia Odonto-onycho dysplasia-alopecia syndrome Autosomal ichthyosis syndrome with prominent neurologic signs Odontotrichomelic syndrome MEDNIK syndrome Papillon-Lefèvre syndrome Hereditary hypotrichosis with recurrent skin vesicles Johanson-Blizzard syndrome Johnson neuroectodermal syndrome Acrofacial dysostosis, Weyers type Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome Sjögren-Larsson syndrome Autosomal recessive congenital ichthyosis Peeling skin syndrome EEC syndrome and related disorders Autosomal ichthyosis syndrome with other associated signs Genetic hair anomaly Dyskeratosis congenita Autosomal recessive palmoplantar keratoderma and congenital alopecia CHILD syndrome Epidermolysis bullosa simplex due to BP230 deficiency Taurodontia-absent teeth-sparse hair syndrome Barber-Say syndrome Keratinopathic ichthyosis Bartsocas-Papas syndrome Epidermolysis bullosa simplex with anodontia/hypodontia Autosomal ichthyosis syndrome with fatal disease course Hypotrichosis simplex Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome