Phenotypes for disease #00896 (DWS (Dandy-Walker syndrome (DWS)), OMIM:220200)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Diagnosis     

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Individual ID     
0000358325 Developmental delay, severe; Speech delay; Mental retardation, moderate to severe; Seizures; Microcephaly; Hypotonia; Agitation; Micrognathia; Strabismus; Optic atrophy, bilateral; Early eruption of teeth; Large ears; Joints laxity; Flexed elbow; Extended feet; Feeding problem and very thin built. Brain MRI revealed hypoplasia of inferior vermis suggestive of dandy walker spectrum Dandy-Walker malformation, brain abnormalities - Familial, autosomal recessive 5y - - - - Johan den Dunnen 00473530
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