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bn:00488870n
Noun Concept
Categories: Genodermatoses, Syndromes affecting the eye, Autosomal recessive disorders, Diseases named for discoverer, Syndromes affecting stature
EN
Rothmund-Thomson syndrome  Rothmund–Thomson syndrome  Congenital poikiloderma  Erythrokeratoderma  Poikiloderma Atrophicans and Cataract
EN
Rothmund–Thomson syndrome is a rare autosomal recessive skin condition. Wikipedia
Definitions
Relations
Sources
EN
Rothmund–Thomson syndrome is a rare autosomal recessive skin condition. Wikipedia
Human disease Wikidata
IS A
rare disease
skin disease
hereditary cancer syndrome
photodermatosis
DNA repair-deficiency disorder
+1 relations
GENETIC ASSOCIATION
RECQL4
HEALTH SPECIALTY
medical genetics
Wikipedia
EN
Rothmund–Thomson syndrome
Wikidata
EN
Rothmund-Thomson syndrome
Wikipedia Redirections
EN
Erythrokeratoderma, poikiloderma congenitale, Poikiloderma of Rothmund-Thomson, Poikiloderma of Rothmund–Thomson, Rothmund-Thompson's syndrome, Rothmund-Thompson syndrome, Rothmund-Thomson Syndrome, Rothmund thomson syndrome, Symmetrical progressive of Gottron erythrokeratoderma, Thomson Syndome, Thomson syndrome
Wikidata Alias
EN
Congenital poikiloderma, Poikiloderma Atrophicans and Cataract, Poikiloderma of Rothmund-Thomson, ROTHMUND-THOMSON SYNDROME, ROTHMUND-THOMSON SYNDROME; RTS, RTS, Rothmund-Thomson syndrome (disorder)

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