Phenotypes for disease #00626 (BRWS1 (Baraitser-Winter syndrome, type 1 (BRWS1)), OMIM:243310)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000087496 Severe ID, congenital heart defect, cleft lip and palate, epilepsy, behavioural anomalies, dysplastic ears, pre-auricular pit, downslanting palpebral fissures - - Isolated (sporadic) - - - - - Bernt Popp 00111411
0000152806 see paper; ... - BRWS-1 Isolated (sporadic) - - - - - Jennifer Johnston 00204316
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