Phenotypes for disease #05405 (SKDEAS (Skraban-Deardorff syndrome (SKDEAS)), OMIM:617616)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000223189 WDR26 haploinsufficiency WDR26 haploinsufficiency Clinical features of our patient were intellectual disability with delayed speech, developmental delay, gait abnormalities, and characteristic facial phenotype, but absence of seizures and autism. Familial, autosomal dominant 10y09m 11y 01y developmental delay WDR26 Wenjuan Qiu 00295623
0000325439 - - Synophrys, Motor delay, Delayed speech and language development, Ventriculomegaly Unknown 01y - - - - Andreas Laner 00435243
0000333161 - - Autistic behavior, Delayed speech and language development, Generalized non-motor (absence) seizure, Neurodevelopmental delay Isolated (sporadic) 05y - - - - Andreas Laner 00443884
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