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Human Disease and Mouse Model Detail
Human Disease Mitochondrial DNA Depletion Syndrome 4a (alpers Type); MTDPS4A
OMIM ID: 203700
Human Phenotype Ontology associations
Synonyms Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis; Alpers Progressive Infantile Poliodystrophy; Alpers Syndrome; Alpers-Huttenlocher Syndrome; Mitochondrial DNA Depletion Syndrome; Neuronal Degeneration of Childhood with Liver Disease, Progressive; PNDC
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
     POLG* Polg   HomoloGene and HGNC

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
MGI 6.07
The Jackson Laboratory