Cortical Dysplasia, Complex, With Other Brain Malformations 2; Cdcbm2
Genes related to Cortical Dysplasia, Complex, With Other Brain Malformations 2; Cdcbm2
- KIF5C
Clinical Features
Top most frequent phenotypes and symptoms related to Cortical Dysplasia, Complex, With Other Brain Malformations 2; Cdcbm2
- Intellectual disability
- Seizures
- Global developmental delay
- Microcephaly
- Growth delay
- Abnormal facial shape
- Intrauterine growth retardation
- Hypoplasia of the corpus callosum
- Hypertonia
- Absent speech
And another 10 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Cortical Dysplasia, Complex, With Other Brain Malformations 2; Cdcbm2 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Cerebral Cortical Malformation Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
SNAP29, TUBA8, TUBB2A, TUBG1, VLDLR, ACTB, RAB18, ACTG1, B3GNT2, B4GAT1, CCND2, ARFGEF2, TBC1D20, RAB3GAP1, RAB3GAP2, NDE1, CDK5, FKRP, ARX, ATP6V0A2 , (...)
View the complete list with 34 more genes
Specificity
2 %
Genes
100 % |
Lissencephaly Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
SNAP29, TUBG1, VLDLR, ACTB, RXYLT1, ACTG1, B4GAT1, NDE1, CDK5, FKRP, ARX, ATP6V0A2, POMGNT1, POMT2, TUBA1A, TUBB3, TUBB, GMPPB, SRD5A3, POMGNT2 , (...)
View the complete list with 16 more genes
Specificity
3 %
Genes
100 % |
Comprehensive Lissencephaly Panel.
By Genetic Services Laboratory University of Chicago (United States).
SNAP29, TUBG1, VLDLR, ACTB, RXYLT1, ACTG1, B4GAT1, CDK5, FKRP, ARX, ATP6V0A2, POMGNT1, POMT2, TUBA1A, TUBB3, TUBB, GMPPB, SRD5A3, POMK, DCX , (...)
View the complete list with 14 more genes
Specificity
3 %
Genes
100 % |
Cerebral Cortical Malformations Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
SNAP29, TUBA8, TUBB2A, TUBG1, VLDLR, ACTB, RAB18, ACTG1, B3GNT2, B4GAT1, CCND2, ARFGEF2, TBC1D20, RAB3GAP1, RAB3GAP2, NDE1, CDK5, FKRP, ARX, ATP6V0A2 , (...)
View the complete list with 34 more genes
Specificity
2 %
Genes
100 % |
Cortical dysplasia, complex, with other brain malformations 2 (sequence analysis of KIF5C gene).
By CGC Genetics (Portugal).
KIF5C
Specificity
100 %
Genes
100 % |
Microcephaly and pontocerebellar hypoplasia (NGS panel for 52 genes).
By CGC Genetics (Portugal).
STIL, BUB1B, TUBG1, VRK1, SLC25A19, NIN, CASK, TSEN34, ZNF335, PCNT, STAMBP, CLP1, CENPJ, NDE1, EXOSC3, TUBGCP6, IER3IP1, CDK5RAP2, ASPM, MBD5 , (...)
View the complete list with 32 more genes
Specificity
2 %
Genes
100 % |
Lissencephaly and related disorders NGS test.
By Connective Tissue Gene Tests (United States).
SNAP29, TUBA8, TUBB2A, TUBG1, VLDLR, ACTB, RXYLT1, ACTG1, B4GAT1, NDE1, CDK5, FKRP, ARX, ATP6V0A2, POMGNT1, POMT2, TUBA1A, TUBB3, TUBB, GMPPB , (...)
View the complete list with 22 more genes
Specificity
3 %
Genes
100 % |
Lissencephaly and related disorders Deletion / Duplication test.
By Connective Tissue Gene Tests (United States).
SNAP29, TUBA8, TUBB2A, TUBG1, VLDLR, ACTB, RXYLT1, ACTG1, B4GAT1, NDE1, CDK5, FKRP, ARX, ATP6V0A2, POMGNT1, POMT2, TUBA1A, TUBB3, TUBB, GMPPB , (...)
View the complete list with 22 more genes
Specificity
3 %
Genes
100 % |
You can get up to 11 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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