early infantile epileptic encephalopathy 9 (Q3813663)
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infantile epileptic encephalopathy that has material basis in the gene encoding protocadherin-19 (PCDH19) on chromosome Xq22
- Juberg Hellman syndrome
- female restricted epilepsy with mental retardation
- EFMR
- early infantile female-limited epilecptic encephalopathy
- EIEE9
- PCDH19 related syndrome
- PCDH19 Epilepsy
- Epilepsy and mental retardation limited to females
- PCDH19 female pediatric epilepsy
- PCDH19-related epilepsy
- Protocadherin 19 (PCDH19)-related epilepsy
- Epilepsy-intellectual disability in females
- developmental and epileptic encephalopathy 9
- DEE9
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | early infantile epileptic encephalopathy 9 |
infantile epileptic encephalopathy that has material basis in the gene encoding protocadherin-19 (PCDH19) on chromosome Xq22 |
|
Statements
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17 May 2019
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C201590
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Identifiers
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