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Parent Node:
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Hypobetalipoproteinemias (D006995)
..Starting node
..expand
Nguyen syndrome (C536115)

       Child Nodes:



 Sister Nodes: 
..expandAbetalipoproteinemia (D000012) Child2
..expandChylomicron retention disease (C535460)
..expandHypobetalipoproteinemia, Familial, 2 (C565732)
..expandHypobetalipoproteinemia, Familial, Apolipoprotein B (D052476) Child1
..expandNguyen syndrome (C536115)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:8910
Name:Nguyen syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D006995
TreeNumbers:C16.320.565.398.500.440/C536115 |C18.452.584.500.875.440/C536115 |C18.452.648.398.500.440/C536115
Synonyms:
Slim Mappings:Genetic disease (inborn)|Metabolic disease
Reference: MedGen: C536115
MeSH: C536115
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal