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bn:03430533n
Noun Concept
Categories: Syndromes affecting the tongue, Congenital disorders of musculoskeletal system, Syndromes affecting the jaw, Diseases named for discoverer, Syndromes with craniofacial abnormalities
EN
Pierre Robin sequence  Pierre Robin syndrome  Pierre-Robin syndrome  Pierre Robin's sequence  Pierre Robin's syndrome
EN
Pierre Robin sequence is a congenital defect observed in humans which is characterized by facial abnormalities. Wikipedia
Definitions
Relations
Sources
EN
Pierre Robin sequence is a congenital defect observed in humans which is characterized by facial abnormalities. Wikipedia
A congenital condition of facial abnormalities Wikipedia Disambiguation
A congenital condition with micrognathia and glossoptosis Wikidata
IS A
disease
sequence
First arch syndrome
HAS KIND
Weissenbacher-Zweymuller syndrome
Catel–Manzke syndrome
HEALTH SPECIALTY
medical genetics
NAMED AFTER
Pierre Robin
SYMPTOMS
glossoptosis
Wikipedia
EN
Pierre Robin sequence
Wikidata
EN
Pierre Robin syndrome
Wikipedia Redirections
EN
Pierre-Robin syndrome, Pierre Robin's sequence, Pierre Robin's syndrome, Pierre Robin syndrome, Pierre Robins sequence, Pierre Robins syndrome, Robin sequence and oligodactyly, Robin syndrome
Wikidata Alias
EN
Pierre Robin anomalad, Pierre Robin anomaly, Pierre Robin malformation, Pierre Robin sequence

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