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Stromme syndrome

Disease Summary
Associated Targets (1)
Tbio

1


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Mondo Description Stromme syndrome is an autosomal recessive congenital disorder affecting multiple systems with features of a ciliopathy. Affected individuals typically have some type of intestinal atresia, variable ocular abnormalities, microcephaly, and sometimes involvement of other systems, including renal and cardiac. In some cases, the condition is lethal in early life, whereas other patients show normal survival with or without mild cognitive impairment (summary by Filges et al., 2016).
Uniprot Description An autosomal recessive congenital disorder characterized by intestinal atresia, ocular anomalies, microcephaly, and renal and cardiac abnormalities in some patients. The disease has features of a ciliopathy, and lethality in early childhood is observed in severe cases.
Mondo Term and Equivalent IDs
MONDO:0009477:  Stromme syndrome
EFO:0009160: 
MESH:C565460: 
Orphanet:444069: 
Orphanet:506307: 
UMLS:CN237682: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)
No novelty measurements found