Phenotypes for disease #05770 (KLEFS2 (Kleefstra syndrome, type 2 (KLEFS2)), OMIM:617768)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000291700 prenatal (SSW 12+6) - Increased nuchal translucency (5,3 mm) Isolated (sporadic) - - - - Andreas Laner 00398613
0000291701 SSW12+6 - Increased nuchal translucency (5,3 mm) Isolated (sporadic) - - - - Andreas Laner 00398614
0000346963 - - Global developmental delay, Atypical behavior, Exodeviation, Aggressive behavior, Expressive language delay Unknown 05y - - - Andreas Laner 00458528
0000346964 - - Global developmental delay, Atypical behavior, Exodeviation, Aggressive behavior, Expressive language delay Unknown 05y - - - Andreas Laner 00458529
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