Neurodegeneration and seizures due to copper transport defect

Preferred Label : Neurodegeneration and seizures due to copper transport defect;

Symbol : NSCT;

Type : Phenotype, molecular basis known;

Prefixed ID : #620306;

Details

Origin ID

620306;

UMLS CUI

C5830385;

Genes related to phenotype
- Solute carrier family 31 (copper transporter), member 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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