Phenotypes for disease #01012 (BRWS2 (Baraitser-Winter syndrome, type 2 (BRWS2)), OMIM:614583)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000219688 no short stature, no microcephaly postnatal; intellectual disability, hearing loss, seizures; trigonocephaly, hypertelorism, high-arched eyebrows, congenital ptosis; no coloboma; pachygyria only anterior greater than posterior lissencephaly Baraitser-Winter syndrome BRWS2 Isolated (sporadic) - - - - - Johan den Dunnen 00204328
0000220841 - - - Isolated (sporadic) 02y06m - - - - Camille Cenni 00287104
0000310963 Global developmental delay - - Isolated (sporadic) 02y - - - - Andreas Laner 00419683
0000346560 see paper; ... Baraitser-Winter syndrome BRWS2 Isolated (sporadic) - - - - - Ludovico Graziani 00458115
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