X-Linked Lissencephaly 1
Disease ID: disease_node_19264
Connections displayed (default: 10).
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| Dbxref | MIM:300067 |
|---|---|
| Subclassof | DOID_0050453, DOID_0050735 |
| Data Source | DOID |
| Synonyms | XLIS1, lissencephaly type 1 due to doublecortin gene mutation |
| Doid Label | X-linked lissencephaly 1 |
| Doid Description | A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23. |
| Has Material Basis In | GENO_0000936 |
| Disease Node Id | disease_node_19264 |
| Doid Id | DOID_0112239 |
| Label | X-Linked Lissencephaly 1 |
- Outgoing r'ship
SUBCLASS_OFto/from X-Linked Monogenic Disease(ID:disease_node_13360) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Lissencephaly(ID:disease_node_11852) (Disease)