Nemaline myopathy 5b, autosomal recessive, childhood-onset

Preferred Label : Nemaline myopathy 5b, autosomal recessive, childhood-onset;

Symbol : NEM5B;

Type : Phenotype, molecular basis known;

Prefixed ID : #620386;

Details

Origin ID

620386;

UMLS CUI

C5830545;

Genes related to phenotype
- Troponin t1, skeletal, slow [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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