Disease #00342 (LISX-1;SCLH (lissencephaly, X-linked, type 1 (LISX-1, subcortical laminar heterotopia (SCLH))), OMIM:300067)
| Official abbreviation |
LISX-1;SCLH |
| Name |
lissencephaly, X-linked, type 1 (LISX-1, subcortical laminar heterotopia (SCLH)) |
| OMIM ID |
300067 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DCX |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-03-12 20:58:51 +01:00 (CET) |
| Date last edited |
N/A |
|
