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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