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Human Disease and Mouse Model Detail
Human Disease Gracile Syndrome
OMIM ID: 603358
Synonyms Fellman Syndrome; Finnish Lethal Neonatal Metabolic Syndrome; FLNMS; Growth Retardation, Amino Aciduria, Cholestasis, Iron Overload, Lactic Acidosis, and Early Death; Lactic Acidosis, Finnish, with Hepatic Hemosiderosis
View all models View ALL (1) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Bcs1l* BCS1L* View 1 model 1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory