Disease #00266 (LISX-2;XLAG (lissencephaly, X-linked, type 2 (LISX-2, with ambiguous genitalia (XLAG))), OMIM:300215)
| Official abbreviation |
LISX-2;XLAG |
| Name |
lissencephaly, X-linked, type 2 (LISX-2, with ambiguous genitalia (XLAG)) |
| OMIM ID |
300215 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ARX |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-11-02 13:54:37 +01:00 (CET) |
| Date last edited |
N/A |
|
