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bn:23507890n

Noun Concept

Categories: Rare syndromes, Syndromes affecting the kidneys, Syndromes affecting head size, Ciliopathy, Syndromes affecting the gastrointestinal tract

Stromme syndrome Strømme syndrome apple peel syndrome with microcephaly and ocular anomalies CILD31 jejunal atresia with microcephaly and ocular anomalies

Strømme syndrome is a very rare autosomal recessive genetic condition characterised by intestinal atresia, eye abnormalities and microcephaly. Wikipedia

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Strømme syndrome is a very rare autosomal recessive genetic condition characterised by intestinal atresia, eye abnormalities and microcephaly. Wikipedia

human disease Wikidata

IS A

rare disease

duodenal atresia

primary ciliary dyskinesia

GENETIC ASSOCIATION

CENPF

HEALTH SPECIALTY

medical genetics

Wikipedia

Strømme syndrome

Wikidata

Stromme syndrome

Wikipedia Redirections

Stromme syndrome

Wikidata Alias

apple peel syndrome with microcephaly and ocular anomalies, CILD31, jejunal atresia with microcephaly and ocular anomalies, lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome, primary ciliary dyskinesia 31, Stromme Syndrome