Human genes for copper deficiency myelopathy
Copper deficiency myelopathy [DOID:5112]
A nutritional deficiency disease that is characterized by deficiency of copper, causing spastic gait and ataxia, often with anemia and neutropenia, has_symptom imbalance and jerking movements, and has_material_basis_in copper deficiency possibly due to malabsorption or excess zinc ingestion.
Synonyms: copper deficiency myelopathy, copper deficiency myelopathies, DOID:5112, human swayback, human swaybacks