 QA0.01 |
|
Neurodevelopmental disorders related to pathogenic variants in certain specific genes |
| |
| QA0.010 |
|
Neurodevelopmental disorders, related to pathogenic variants in ion channel genes |
| |
 QA0.0101 |
|
SCN2A-related neurodevelopmental disorder |
| | |
| QA0.0102 |
|
CACNA1A-related neurodevelopmental disorder |
| | |
| QA0.0109 |
 |
Neurodevelopmental disorder related to pathogenic variant in other ion channel gene |
| |
| SCN8A-related neurodevelopmental disorder |
|
| |
| |
| QA0.011 |
|
Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes |
|
| |
| QA0.012 |
|
Neurodevelopmental disorders, related to pathogenic variants in other receptor genes |
|
| |
| QA0.013 |
|
Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes |
| |
| QA0.0131 |
|
SLC6A1-related disorder |
| |
| GABA transporter 1 deficiency |
|
| | |
| QA0.0139 |
|
Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene |
| |
| |
| QA0.014 |
|
Neurodevelopmental disorders, related to pathogenic variants in synapse related genes |
| |
| QA0.0141 |
|
Syntaxin-binding protein 1-related disorder |
| |
|
| | |
| QA0.0142 |
|
DLG4-related synaptopathy |
| | |
| QA0.0149 |
|
Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene |
| |
| Other genetic synaptopathy |
|
| |
| |
| QA0.015 |
|
Neurodevelopmental disorders, related to genes associated with transcription and gene expression |
| |
| QA0.0151 |
|
FOXG1 syndrome |
| |
| FOXG1-related disorder | | FOXG1-related encephalopathy | | FOXG1-related neurodevelopmental disorder |
|
| | |
| QA0.0159 |
|
Neurodevelopmental disorder, related to other genes associated with transcription and gene expression |
| |
