1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0112107 | McLeod syndrome | A neuroacanthocytosis characterized by absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, compensated hemolysis, and involuntary movements that has_material_basis_in mutation in XK on chromosome Xp21.1. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:1289 | neurodegenerative disease | A central nervous system disease that results in the progressive deterioration of function or structure of neurons. |
