SE-ATLAS

Hypertrichosis-acromegaloid facial appearance syndrome Epidermolysis bullosa simplex due to exophilin 5 deficiency Congenital cataract-ichthyosis syndrome Congenital ichthyosiform erythroderma Autosomal dominant generalized epidermolysis bullosa simplex, severe form ANE syndrome Keratoderma hereditarium mutilans with ichthyosis Familial isolated trichomegaly Alopecia totalis Epidermolysis bullosa simplex with mottled pigmentation Localized epidermolysis bullosa simplex Alopecia universalis Acral self-healing collodion baby Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form Intermediate generalized junctional epidermolysis bullosa Ichthyosis-hypotrichosis syndrome PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement Localized junctional epidermolysis bullosa Severe generalized junctional epidermolysis bullosa Self-improving collodion baby Sparse hair-short stature-skin anomalies syndrome Junctional epidermolysis bullosa with pyloric atresia Pili torti Late-onset junctional epidermolysis bullosa Ito hypomelanosis Junctional epidermolysis bullosa inversa Pili torti-developmental delay-neurological abnormalities syndrome Focal facial dermal dysplasia type I Monilethrix 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 Woolly hair Focal facial dermal dysplasia type III Marie Unna hereditary hypotrichosis Woolly hair nevus Osteosclerosis-ichthyosis-premature ovarian failure syndrome Generalized peeling skin syndrome Pili bifurcati Acquired hypertrichosis lanuginosa Autosomal dominant epidermolytic ichthyosis Basal epidermolysis bullosa simplex Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Peeling skin syndrome type A Lamellar ichthyosis Suprabasal epidermolysis bullosa simplex Annular epidermolytic ichthyosis Peeling skin syndrome type B Focal facial dermal dysplasia type II Kindler epidermolysis bullosa Erythrokeratodermia variabilis Hair defect-photosensitivity-intellectual disability syndrome Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome Uncombable hair syndrome Peeling skin syndrome type C Localized dystrophic epidermolysis bullosa, acral form Bathing suit ichthyosis Harlequin ichthyosis Localized dystrophic epidermolysis bullosa, nails only Alopecia antibody deficiency Recessive X-linked ichthyosis Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Epidermolysis bullosa simplex with circinate migratory erythema Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Trichorhinophalangeal syndrome type 1 Epidermolysis bullosa simplex with pyloric atresia Crandall syndrome Focal facial dermal dysplasia type IV Frontonasal dysplasia-alopecia-genital anomalies syndrome Congenital generalized hypertrichosis, Ambras type CEDNIK syndrome Quinquaud folliculitis decalvans Cleft lip/palate-ectodermal dysplasia syndrome Atrichia with papular lesions Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Hypotrichosis simplex of the scalp Tricho-oculo-dermo-vertebral syndrome Autosomal dominant trichoodontoonychodysplasia-syndactyly Ichthyosis-cheek-eyebrow syndrome Trichodysplasia-xeroderma syndrome Laryngo-onycho-cutaneous syndrome Netherton syndrome Congenital ichthyosis-microcephalus-tetraplegia 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 Epidermolysis bullosa simplex superficialis Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form Graham Little-Piccardi-Lassueur syndrome Dystrophic epidermolysis bullosa pruriginosa Centripetalis recessive dystrophic epidermolysis bullosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Ichthyosis-prematurity syndrome Noonan syndrome-like disorder with loose anagen hair Pili gemini Ichthyosis Autosomal dominant generalized dystrophic epidermolysis bullosa Lichen planopilaris X-linked congenital generalized hypertrichosis Inherited epidermolysis bullosa Ichthyosis hystrix gravior Autosomal ichthyosis syndrome with prominent hair abnormalities Syndromic hair shaft abnormality Ichthyosis hystrix of Curth-Macklin Rare disorder with hypertrichosis Syndromic recessive X-linked ichthyosis Isolated hair shaft abnormality Björnstad syndrome Autosomal dominant deafness-onychodystrophy syndrome Alopecia Frontal fibrosing alopecia DOORS syndrome Epidermolysis bullosa simplex with muscular dystrophy Alopecia-intellectual disability syndrome Isolated anterior cervical hypertrichosis Lethal acantholytic erosive disorder Inherited ichthyosis syndromic form Cervical hypertrichosis-peripheral neuropathy syndrome X-linked dominant chondrodysplasia punctata Superficial epidermolytic ichthyosis Cooks syndrome Pseudopelade of Brocq Autosomal ichthyosis syndrome with prominent neurologic signs MEDNIK syndrome Hereditary hypotrichosis with recurrent skin vesicles Sjögren-Larsson syndrome Autosomal recessive congenital ichthyosis Peeling skin syndrome Autosomal ichthyosis syndrome with other associated signs Genetic hair anomaly CHILD syndrome Epidermolysis bullosa simplex due to BP230 deficiency Taurodontia-absent teeth-sparse hair syndrome Keratinopathic ichthyosis Epidermolysis bullosa simplex with anodontia/hypodontia Autosomal ichthyosis syndrome with fatal disease course Hypotrichosis simplex