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Human Disease

mitochondrial DNA depletion syndrome 15

Term ID
DOID:0080337
Synonyms
Definition
A mitochondrial DNA depletion syndrome that is characterized by severe intrauterine growth restriction, neonatal-onset hypoglycemia and liver dysfunction, mitochondrial DNA depletion in liver and skeletal muscle, and abnormal mitochondrial morphology observed in skeletal muscle, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the mitochondrial transcription factor A gene on chromosome 10q21. (3)
References
Ontology
Human Disease   ( DOID:0080337 )
Relationships
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Genes Involved
Zebrafish Models