Hyperferritinemia

Preferred Label : Hyperferritinemia;

Symbol : HRFT;

Type : Phenotype, molecular basis known;

Prefixed ID : #620729;

Origin ID

620729;

UMLS CUI

C3854388;

Genes related to phenotype
- Stabilin 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperferritinaemia [MedDRA Preferred Term]
- Hyperferritinemia [MeSH Descriptor]
- Hyperferritinemia [MedDRA LLT]
- hyperferritinemia [Disease (Nov.)]