MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5 - OMIM Mitochondrial complex IV deficiency nuclear type 5 (MC4DN5) is an autosomal recessive severe metabolic multisystemic disorder with onset in infancy Features include delayed psychomotor development, impaired intellectual development with speech delay, mild dysmorphic facial features, hypotonia, ataxia, and seizures
MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5 - OMIM Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes
220111 NAPA Gold AIR FILTER Engine Crankcase Breather Element . . . - eBay The part number for this air filter is 220111 NAPA and it is compatible with various interchange part numbers such as SA12623, 93387, and WS10111 It is suitable for use in cars and trucks and falls under the category of exhaust and emission systems
Premature Ovarian Failure in French Canadian Leigh Syndrome Leigh Syndrome, French-Canadian variety (LSFC, OMIM # 220111), is an autosomal recessive mitochondrial disease caused by mutations in the gene encoding leucine-rich pentatricopeptide repeat domain containing protein (LRPPRC) on chromosome 2p21
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