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| Genetic Epilepsy v0.1223 | ALX4 | Zornitza Stark Marked gene: ALX4 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1223 | ALX4 | Zornitza Stark Gene: alx4 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1223 | ALX4 |
Zornitza Stark gene: ALX4 was added gene: ALX4 was added to Genetic Epilepsy. Sources: Expert Review Mode of inheritance for gene: ALX4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ALX4 were set to 33269135 Phenotypes for gene: ALX4 were set to Parietal foramina 2, MIM# 609597 Review for gene: ALX4 was set to RED Added comment: Single case report of seizures in an individual with ALX4 variant and parietal foramina, unclear if related. Sources: Expert Review |
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