Human Disease and Mouse Model Detail
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Human Disease
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Mitochondrial DNA Depletion Syndrome 4a (alpers Type); MTDPS4A
OMIM ID: 203700
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Synonyms
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Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis;
Alpers Progressive Infantile Poliodystrophy;
Alpers Syndrome;
Alpers-Huttenlocher Syndrome;
Neuronal Degeneration of Childhood with Liver Disease, Progressive; PNDC
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Polg
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POLG*
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1:1 Homology
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Analysis Tools