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bn:03284294n
Noun Concept
Categories: Rare diseases, Transcription factor deficiencies, Growth disorders
EN
Léri–Weill dyschondrosteosis  dyschondrosteosis  Leri-Weil syndrome  Leri-Weill disease  Leri-Weill dyschondrosteosis
EN
Léri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs and a bayonet-like deformity of the forearms. Wikipedia
Definitions
Relations
Sources
EN
Léri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs and a bayonet-like deformity of the forearms. Wikipedia
Human disease Wikidata
IS A
osteochondrodysplasia
HEALTH SPECIALTY
medical genetics
NAMED AFTER
André Léri
Wikipedia
EN
Léri–Weill dyschondrosteosis
Wikidata
EN
Léri–Weill dyschondrosteosis
Wikipedia Redirections
EN
dyschondrosteosis, Leri-Weil syndrome, Leri-Weill disease, Leri-weill dyschondrosteosis, Leri-Weill dyschondrosteosis, Leri-Weill syndrome, Leri weill dyschondrosteosis, Leri Weill Syndrome, Leri–Weill dyschondrosteosis, Léri-Weill disease, Léri-Weill dyschondrosteosis, Léri-Weill syndrome
Wikidata Alias
EN
Leri-Weill dyschondrosteosis, Léri-Weill dyschondrosteosis

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