Metadata | |
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ID | DOID:0112087 |
Name | nuclear type mitochondrial complex I deficiency 23 |
Definition | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA12 gene on chromosome 12q22. https://pubmed.ncbi.nlm.nih.gov/21617257/ |
Xrefs | |
Synonyms |
MC1DN23 [EXACT] |
Parent Relationships | |
Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |