Adapted from CDC Oestrus ovis First instar larva of O. ovis, collected from the eye of a patient in India presenting with conjunctivitis. Image courtesy of the L V Prasad Eye Institute, Banjara Hills, India. [wikidoc.org]

• Anemia

  Other Species mRNA Descriptions Other Names GeneReviews Methods Data last updated at UCSC: 2023-02-17 13:02:02 MalaCards Disease Associations MalaCards Gene Search: MT-CO1 Diseases sorted by gene-association score: acquired idiopathic sideroblastic anemia [genome.cse.ucsc.edu]

• Abdominal Distension

  Mary's Hospital with the complaints of intermittent indigestion and abdominal distension nearly for 1 year. Laboratory findings appeared almost normal except increased eosinophils up to 14 per cent. [pesquisa.bvsalud.org]

• Night Blindness

  blindness, congenital stationary, 1a, x-linked (9), parasitic helminthiasis infectious disease (8), fatal infantile encephalocardiomyopathy (8), ophthalmomyiasis (8), retinitis pigmentosa-40 (8), cardiomyopathy, hypertrophic, 2 (7), myasthenic syndrome [genome.cse.ucsc.edu]

• Myopathy

  infantile, transient 9.8 MT-ND1 MT-CO1 12 mitochondrial myopathy 9.8 MT-ND1 MT-CO1 13 myiasis 9.8 MT-ND1 MT-CO1 14 deafness, nonsyndromic sensorineural, mitochondrial 9.8 MT-ND1 MT-CO1 15 alveolar echinococcosis 9.8 MT-ND1 MT-CO1 16 taeniasis 9.8 MT-ND1 [malacards.org]

  […] recurrent* (400), mitochondrial complex iv deficiency* (341), mitochondrial non-syndromic sensorineural deafness* (247), genetic recurrent myoglobinuria* (247), deafness, mitochondrial, modifier of* (202), familial colorectal cancer* (200), mitochondrial myopathy [genome.cse.ucsc.edu]

• Suggestibility

  Life Cycle Most evidence suggests three hosts (including an arthropod intermediate host, a vertebrate intermediate host, and a carnivore definitive host) are required for completion of the life cycle of Mesocestoides spp. [cdc.gov]

• Stroke

  MT-CO1 23 mitochondrial disease 9.8 MT-ND1 MT-CO1 24 mitochondrial encephalomyopathy 9.8 MT-ND1 MT-CO1 25 optic nerve disease 9.8 MT-ND1 MT-CO1 26 kearns-sayre syndrome 9.8 MT-ND1 MT-CO1 27 mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like [malacards.org]

  […] deficiency* (341), mitochondrial non-syndromic sensorineural deafness* (247), genetic recurrent myoglobinuria* (247), deafness, mitochondrial, modifier of* (202), familial colorectal cancer* (200), mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like [genome.cse.ucsc.edu]

• Encephalopathy

  […] associated with ragged-red fibers 9.8 MT-ND1 MT-CO1 23 mitochondrial disease 9.8 MT-ND1 MT-CO1 24 mitochondrial encephalomyopathy 9.8 MT-ND1 MT-CO1 25 optic nerve disease 9.8 MT-ND1 MT-CO1 26 kearns-sayre syndrome 9.8 MT-ND1 MT-CO1 27 mitochondrial myopathy, encephalopathy [malacards.org]

  mitochondrial complex iv deficiency* (341), mitochondrial non-syndromic sensorineural deafness* (247), genetic recurrent myoglobinuria* (247), deafness, mitochondrial, modifier of* (202), familial colorectal cancer* (200), mitochondrial myopathy, encephalopathy [genome.cse.ucsc.edu]

• Meningism

  […] encephalocardiomyopathy (8), ophthalmomyiasis (8), retinitis pigmentosa-40 (8), cardiomyopathy, hypertrophic, 2 (7), myasthenic syndrome, congenital, 10 (7), mcardle disease (7), hymenolepiasis (7), paragonimiasis (7), cercarial dermatitis (7), cysticercosis (6), chronic meningitis [genome.cse.ucsc.edu]

It was failed to reveal the scolex by the first evacuation, but one among 3 worms evacuated by the treatment with atabrine and enough purgations 2 months later, has been found the characteristic scolex. [pesquisa.bvsalud.org]