retinitis pigmentosa, juvenile, Aipl1-Related

Preferred Label : retinitis pigmentosa, juvenile, Aipl1-Related;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0568122;

UMLS CUI

C2751763;

Automatic exact mappings (from CISMeF team)
- Leber congenital amaurosis 4 [OMIM Phenotype]
Related record
- leber congenital amaurosis 4 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]