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bn:23507890n
Noun Concept
SYL
No term available
EN
Strømme syndrome is a very rare autosomal recessive genetic condition characterised by intestinal atresia, eye abnormalities and microcephaly. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
duodenal atresia
EN
primary ciliary dyskinesia
GENETIC ASSOCIATION
EN
CENPF
HEALTH SPECIALTY
EN
medical genetics

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