Bardet-Biedl syndrome 3

Preferred Label : Bardet-Biedl syndrome 3;

MeSH note : mutation on ARL6IP1 protein, human;

Origin ID

C537911;

UMLS CUI

C1859564;

Automatic exact mappings (from CISMeF team)
- Bardet-biedl syndrome 3 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Bardet-Biedl syndrome 3 [DO Concept]
MeSH term(s) associated for indexing
- bardet-biedl syndrome [MeSH Descriptor]
Record concept(s)
- Bardet-Biedl syndrome 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Bardet-Biedl syndrome 3 [DO Concept]
- Bardet-biedl syndrome 3 [OMIM Phenotype]