Infantile Liver Failure Syndrome 2

Preferred Label : Infantile Liver Failure Syndrome 2;

NCIt definition : An autosomal recessive condition caused by mutation(s) in the NBAS gene, encoding neuroblastoma-amplified sequence. It is characterized by recurrent episodes of acute liver failure that begin in infancy.;

Details

Origin ID

C158135;

UMLS CUI

C3809651;

Currated CISMeF NLP mapping
- Infantile liver failure syndrome 2 [OMIM Phenotype]
See also inter- (CISMeF)
- Interstitial lung and liver disease [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Infantile liver failure syndrome 2 [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- NBAS Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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