crigler najjar syndrome, type 2

Preferred Label : crigler najjar syndrome, type 2;

MeSH note : Crigler Najjar syndrome, type 2;

MeSH synonym : Crigler-Najjar syndrome, type II;

Details

Origin ID

C536213;

UMLS CUI

C2931132;

Automatic exact mappings (from CISMeF team)
- Crigler-Najjar syndrome type II [MedDRA LLT]
- Neutropenia, severe congenital, 2, autosomal dominant [OMIM Phenotype]
Currated CISMeF NLP mapping
- Crigler-Najjar syndrome type 2 [ICD-11 More detail]
- Crigler-Najjar syndrome type 2 [ORDO Disease]
- Crigler-Najjar syndrome, type II (disorder) [SNOMED CT concept]
- Crigler-najjar syndrome, type II [OMIM Phenotype]
- crigler-najjar syndrome, type ii [SNOMED Notion]
MeSH term(s) associated for indexing
- crigler-najjar syndrome [MeSH Descriptor]
ORDO relation(s)
- Crigler-Najjar syndrome type 2 [ORDO Disease]
Record concept(s)
- Crigler Najjar syndrome, type 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Crigler-Najjar syndrome type 2 [ORDO Disease]
- Crigler-Najjar syndrome type 2 [ICD-11 More detail]
- Crigler-Najjar syndrome type II [MedDRA LLT]
- Crigler-Najjar syndrome, type II (disorder) [SNOMED CT concept]
- Crigler-najjar syndrome, type II [OMIM Phenotype]
- crigler-najjar syndrome, type ii [SNOMED Notion]

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