Disease #00138 (autism (autism), OMIM:209850)
| Official abbreviation |
autism |
| Name |
autism |
| OMIM ID |
209850 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
MAGEL2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-06-04 18:17:33 +02:00 (CEST) |
| Date last edited |
N/A |
|