bifid nose with or without anorectal and renal anomalies

Preferred Label : bifid nose with or without anorectal and renal anomalies;

MeSH note : mutations in FREM1;

Origin ID

C567672;

UMLS CUI

C2750433;

Automatic exact mappings (from CISMeF team)
- Bifid nose - anorectal and renal anomalies [ICD-11 More detail]
Currated CISMeF NLP mapping
- BNAR syndrome [ORDO Disease]
- Bifid nose with or without anorectal and renal anomalies [OMIM Phenotype]
- Bifid nose, anorectal anomaly, renal anomaly syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- kidney diseases [MeSH Descriptor]
- nose [MeSH Descriptor]
- rectal diseases [MeSH Descriptor]
Record concept(s)
- bifid nose with or without anorectal and renal anomalies [MeSH concept]
See also
- fraser syndrome [MeSH Descriptor]
- marles greenberg persaud syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- BNAR syndrome [ORDO Disease]
- Bifid nose with or without anorectal and renal anomalies [OMIM Phenotype]
- Bifid nose, anorectal anomaly, renal anomaly syndrome (disorder) [SNOMED CT concept]