Disease #05776 (NEDHAHM (neurodevelopmental disorder, hypotonia and autistic features with/without hyperkinetic movements (NEDHAHM)), OMIM:618760)
| Official abbreviation |
NEDHAHM |
| Name |
neurodevelopmental disorder, hypotonia and autistic features with/without hyperkinetic movements (NEDHAHM) |
| OMIM ID |
618760 |
| 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 |
VAMP2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-06-17 09:53:03 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
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