Amyloidosis, hereditary systemic 5

Preferred Label : Amyloidosis, hereditary systemic 5;

Symbol : AMYLD5;

Type : Phenotype, molecular basis known;

Prefixed ID : #620658;

Details

Origin ID

620658;

UMLS CUI

C5935572;

Genes related to phenotype
- Lysozyme [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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