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Ontology Browser

Term:
mitochondrial complex III deficiency nuclear type 5 (DOID:0080114)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
mitochondrial complex III deficiency nuclear type 1  
Mitochondrial Complex III Deficiency Nuclear Type 10  
mitochondrial complex III deficiency nuclear type 2  
mitochondrial complex III deficiency nuclear type 3  
mitochondrial complex III deficiency nuclear type 4  
mitochondrial complex III deficiency nuclear type 5  
A mitochondrial complex III deficiency characterized by neonatal onset of severe metabolic acidosis associated with hyperammonemia and hypoglycemia and that has_material_basis_in homozygous mutation in the UQCRC2 gene on chromosome 16p12. (DO)
mitochondrial complex III deficiency nuclear type 6  
mitochondrial complex III deficiency nuclear type 7  
mitochondrial complex III deficiency nuclear type 8  
mitochondrial complex III deficiency nuclear type 9  

Synonyms
Exact Synonyms: MC3DN5
Primary IDs: OMIM:615160
Definition Sources: http://omim.org/entry/615160?search=615160&highlight=615160 "DO" "DO"

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