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Human Disease and Mouse Model Detail
Human Disease Neuraminidase Deficiency
OMIM ID: 256550
Human Phenotype Ontology associations
Synonyms Glycoprotein Neuraminidase Deficiency; Lipomucopolysaccharidosis; ML I; Mucolipidosis I; NEU Deficiency; NEUG Deficiency; Neuraminidase 1 Deficiency; Sialidase Deficiency; Sialidosis, Type II
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models 		Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     NEU1* Neu1* View 2 models HomoloGene and HGNC
References Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
09/27/2016
MGI 6.05 		The Jackson Laboratory