Disease #05968 (NEDASB (neurodevelopmental disorder with/without autistic features and/or structural brain abnormalities (NEDASB)), OMIM:618859)
Official abbreviation |
NEDASB |
Name |
neurodevelopmental disorder with/without autistic features and/or structural brain abnormalities (NEDASB) |
OMIM ID |
618859 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
NOVA2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-09-08 13:46:58 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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