Phenotypes for disease #00065 (Rett syndrome (Rett syndrome, congenital variant), OMIM:613454)

36 entries on 1 page. Showing entries 1 - 36.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000029734 - Unknown - - - - - Rett syndrome - congenital - RettBASE 00039451
0000029949 - Unknown - - - - - Rett syndrome - congenital - RettBASE 00039666
0000030038 - Unknown - - - - - Rett syndrome - congenital - RettBASE 00039755
0000030164 - Unknown - - - - - Rett syndrome - congenital - RettBASE 00039881
0000030984 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00040701
0000031236 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00040953
0000031629 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00041346
0000031635 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00041352
0000031640 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00041357
0000031837 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00041554
0000032250 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00041967
0000032251 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00041968
0000032591 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00042308
0000033374 - Unknown - - - - - Rett syndrome - congenital - RettBASE 00043091
0000033676 - Unknown - - - - - Rett syndrome - congenital onset - RettBASE 00043393
0000033729 - Unknown - - - - - Rett syndrome - congenital onset - RettBASE 00043446
0000033980 - Unknown - - - - - Rett syndrome - Congenital onset - RettBASE 00043697
0000050838 - Unknown - - - - - - - Henk van Kranen 00064618
0000060610 - Isolated (sporadic) - - - - - Rett syndrome, congenital variant (OMIM:613454) - Daniel Trujillano 00081041
0000090365 - Unknown - - - - - Rett syndrome? - Emmelien Aten 00114879
0000090381 - Unknown - - - - - Rett syndrome? - Emmelien Aten 00114917
0000090386 - Unknown - - - - - Rett syndrome, variant, infantile spasms; Rett syndrome? - Emmelien Aten 00114927
0000090387 - Unknown - - - - - Rett syndrome? - Emmelien Aten 00114928
0000090388 - Unknown - - - - - Rett syndrome? - Emmelien Aten 00114929
0000090392 - Unknown - - - - - Rett syndrome? - Emmelien Aten 00114933
0000090414 - Unknown - - - - - Rett syndrome, variant, infantile spasms; Rett syndrome? - Emmelien Aten 00114956
0000090417 - Unknown - - - - - Rett syndrome, variant, infantile spasms; Rett syndrome? - Emmelien Aten 00114960
0000090418 - Unknown - - - - - Rett syndrome, atypical; Rett syndrome? - Emmelien Aten 00114961
0000090419 - Unknown - - - - - Rett syndrome? - Emmelien Aten 00114962
0000090429 - Unknown - - - - - Rett syndrome, variant, infantile spasms; Rett syndrome? - Emmelien Aten 00114973
0000090433 - Unknown - - - - - Rett syndrome? - Emmelien Aten 00114885
0000090450 - Unknown 08y? - - 02y? - Rett syndrome - Marianna Kouskou 00114887
0000302570 Rett/Rett-like syndrome Isolated (sporadic) 05y10m DEE72 06y10m 00y08m 8m Microcephaly Hypotonia Gait disturbance Intellectual disability Absent speech Aggressive behavior Partial agenesis of the corpus callosum Absent septum pellucidum not available Edoardo Errichiello 00410464
0000322863 - Isolated (sporadic) - 1y - - - Delayed speech and language development, Delayed gross motor development, Impaired social interactions, Axial hypotonia, Abnormal intestine morphology, Chronic diarrhea, Delayed fine motor development - Andreas Laner 00432295
0000324436 - Isolated (sporadic) - - - - - intellectual disability, developmental delay - Marketa Wayhelova 00434057
0000331428 - Isolated (sporadic) 02y - - - - Autistic behavior, Delayed speech and language development, Neurodevelopmental delay - Andreas Laner 00442049
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