Disease #06947 (NEDSEBA (neurodevelopmental disorder with seizures and brain atrophy), OMIM:619072)
| Official abbreviation |
NEDSEBA |
| Name |
neurodevelopmental disorder with seizures and brain atrophy |
| OMIM ID |
619072 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
EXOC7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-07-18 15:03:57 +02:00 (CEST) |
| Date last edited |
N/A |
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