Disease #07206 (NEDLAAD (neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder), OMIM:620782)
| Official abbreviation |
NEDLAAD |
| Name |
neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder |
| OMIM ID |
620782 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CAPRIN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2025-12-01 11:47:22 +01:00 (CET) |
| Date last edited |
N/A |
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