The following pages link to Template:Genodermatoses-stub
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Polyostotic fibrous dysplasia (transclusion) (links | edit)
- Pachyderma (transclusion) (links | edit)
- Dyschromatosis universalis hereditaria (transclusion) (links | edit)
- Apolipoprotein B deficiency (transclusion) (links | edit)
- DeSanctis–Cacchione syndrome (transclusion) (links | edit)
- Ulerythema (transclusion) (links | edit)
- Elejalde syndrome (transclusion) (links | edit)
- Franceschetti–Klein syndrome (transclusion) (links | edit)
- Cross syndrome (transclusion) (links | edit)
- Ichthyosis linearis circumflexa (transclusion) (links | edit)
- Elastosis perforans serpiginosa (transclusion) (links | edit)
- Keratitis–ichthyosis–deafness syndrome (transclusion) (links | edit)
- Senter syndrome (transclusion) (links | edit)
- Infantile systemic hyalinosis (transclusion) (links | edit)
- Atrichia with papular lesions (transclusion) (links | edit)
- Keratosis pilaris atrophicans faciei (transclusion) (links | edit)
- Atrophodermia vermiculata (transclusion) (links | edit)
- Keratosis follicularis spinulosa decalvans (transclusion) (links | edit)
- Familial progressive hyperpigmentation (transclusion) (links | edit)
- Confluent and reticulated papillomatosis (transclusion) (links | edit)
- Incontinentia pigmenti achromians (transclusion) (links | edit)
- Linear and whorled nevoid hypermelanosis (transclusion) (links | edit)
- Neurofibromatosis type 4 (transclusion) (links | edit)
- Lentiginosis (transclusion) (links | edit)
- Lelis syndrome (transclusion) (links | edit)
- Camisa disease (transclusion) (links | edit)
- Corneodermatoosseous syndrome (transclusion) (links | edit)
- Rapp–Hodgkin syndrome (transclusion) (links | edit)
- Tooth and nail syndrome (transclusion) (links | edit)
- IgA pemphigus (transclusion) (links | edit)
- Transient bullous dermolysis of the newborn (transclusion) (links | edit)
- Pityriasis rotunda (transclusion) (links | edit)
- Ectodermal dysplasia with corkscrew hairs (transclusion) (links | edit)
- Odonto–tricho–ungual–digital–palmar syndrome (transclusion) (links | edit)
- Lenz–Majewski syndrome (transclusion) (links | edit)
- Marie Unna hereditary hypotrichosis (transclusion) (links | edit)
- Hereditary sclerosing poikiloderma (transclusion) (links | edit)
- Mandibuloacral dysplasia (transclusion) (links | edit)
- Generalized trichoepithelioma (transclusion) (links | edit)
- Follicular atrophoderma (transclusion) (links | edit)
- McCusick syndrome (transclusion) (links | edit)
- Keratin disease (transclusion) (links | edit)
- Immunodeficiency with hyperimmunoglobulin M (transclusion) (links | edit)
- Hereditary progressive mucinous histiocytosis (transclusion) (links | edit)
- Inherited patterned lentiginosis (transclusion) (links | edit)
- Relapsing linear acantholytic dermatosis (transclusion) (links | edit)
- Acantholytic dyskeratotic epidermal nevus (transclusion) (links | edit)
- Albinism–deafness syndrome (transclusion) (links | edit)
- Watson syndrome (transclusion) (links | edit)
- Westerhof syndrome (transclusion) (links | edit)