Spastic paraplegia 30b, autosomal recessive

Preferred Label : Spastic paraplegia 30b, autosomal recessive;

Symbol : SPG30B;

Type : Phenotype, molecular basis known;

Prefixed ID : #620607;

Details

Origin ID

620607;

UMLS CUI

C5935571;

Genes related to phenotype
- Kinesin family member 1a [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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