Alfadhel syndrome

Preferred Label : Alfadhel syndrome;

Symbol : AFDL;

Type : Phenotype, molecular basis known;

Prefixed ID : #620655;

Origin ID

620655;

UMLS CUI

C5882735;

Genes related to phenotype
- Rap1, gtpase-gdp dissociation stimulator 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]