Disease #02160 (ASPGX1 (Asperger syndrome X-linked 1), OMIM:300494)
| Official abbreviation |
ASPGX1 |
| Name |
Asperger syndrome X-linked 1 |
| OMIM ID |
300494 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked, Multifactorial, Isolated Cases (Sporadic) |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NLGN3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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