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Qaagi - Book of Why

Causes

Effects

Vitamin B1 , or thiamine deficiencycausesBeriberi disease

various mutations in the ABCA4 gene(passive) is usually caused byStargardt disease

mutations in the gene ABCA4 into the trial(passive) caused byStargardt disease

a mutation in a gene called ABCA4(passive) is caused byStargardt disease

the presence of the recessive genecausesStargardt disease

a rare recessive gene(passive) is caused byStargardt disease

mutations in the ABCA4 gene , which are inherited from both parents(passive) is caused byStargardt disease

mutations in the ABCA4 gene or the ELOVL4 gene(passive) is caused byStargardt disease

mutations affecting the gene represented in this entry(passive) is caused byPRO-196.The disease

mutations in the ATP7A gene.[13(passive) is caused byMenkes disease

mutations in the ELOVL4 gene.[en.wikipedia.org(passive) caused byStargardt disease

mutations in the ABCA4 gene , which is responsible for other retinal dystrophies(passive) is caused byStargardt disease

Over 800 mutations in ABCA4 are now knownto causeStargardt disease

mutations of the ATP7A gene ( 22–24(passive) is caused byMenkes disease

mutations in the ATP7A gene.[9 ] Researchers(passive) is caused byMenkes disease

mutation in the gene encoding Cu(2+)-transporting ATPase(passive) is caused byMenkes disease

a thiamin deficiency(passive) caused byberiberi disease

a defect in the ATP7A gene(passive) is caused byMenkes disease

a change in the ABCA4 genecausesStargardt disease

a faulty ( mutated ) gene(passive) is caused byStargardt disease

a normal copy of the genecausesStargardt disease

mutations in the CTSF gene(passive) caused byKufs disease

mutations in the DNAJC5 gene(passive) caused byKufs disease

Similarly , vitamin B1 is essentialto preventberiberi disease

a mutant gene called ABCR-4.1 They’re working on treatments now(passive) is caused byStargardt disease

faults in a gene known as ABCA4(passive) is caused byStargardt disease

a rare combination of 2 homozygous recessive mutations in the ABCA4 genecausedStargardt disease

thanks Only 2 mutations in the ABCA4 gene ( one from each parent ) are requiredto causeStargardt disease

lack of vitamin B1 ( thiamine(passive) caused byBeriberi , disease

This observation ... an inherited copper deficiencycausesMenkes disease

a defective gene that regulates the metabolism of copper in the body(passive) is caused byMenkes Disease

Currently , over 500 different mutations in ABCA4 are knownto causeStargardt disease

ATP7A gene mutation and Wilson(passive) caused byMenkes disease

just one copy of a gene mutationcausesstargardt disease

mutations in the ABCA 4 genecausesStargardt Disease

the specific changes in the ABCA4 genecausesStargardt disease

One of nineteen mutations in the gene ( causing deletions and substitutions of amino acids ) has been identifiedto causeStargardt disease

seed - borne Fusarium species , mainly F. fujikuroi(passive) caused byBakanae disease

Vitamin B1 is knownto preventberiberi disease

a defect in zinc metabolism that reduces copper availability.20(passive) is caused byMenkes ’ disease

progressive vision loss and blindnesscausesprogressive vision loss and blindness

progressive vision loss usually to the point of legal blindnesscausesprogressive vision loss usually to the point of legal blindness

progressive loss of central visioncausesprogressive loss of central vision

to significant loss of central visionleadsto significant loss of central vision

Vertigo ( dizzinesscan causeVertigo ( dizziness

advanced visual impairment(passive) caused byadvanced visual impairment

progressive vision loss which usually results in the person becoming totally blindcausesprogressive vision loss which usually results in the person becoming totally blind

in inflammation of the bowelcausesin inflammation of the bowel

in severe vision loss in afflicted subjects by age 20typically resultsin severe vision loss in afflicted subjects by age 20

On 1/16/06 5:23 PM by lov2lafCreatedOn 1/16/06 5:23 PM by lov2laf

degenerative partial blindnesscausesdegenerative partial blindness

substantial vision losscan causesubstantial vision loss

blindness in 32 K peoplecausesblindness in 32 K people

the adaptive changes in thyroid hormone action(passive) caused bythe adaptive changes in thyroid hormone action

Repair of septal perforations(passive) caused byRepair of septal perforations

in progressive central vision lossresultsin progressive central vision loss

vision to deteriorate slowly over timecausesvision to deteriorate slowly over time

in periapi - cal inflammation and abscess formationresultingin periapi - cal inflammation and abscess formation

sickle cell disease and vision loss(passive) caused bysickle cell disease and vision loss

vision loss during childhood , adolescence and in some formscausesvision loss during childhood , adolescence and in some forms

vision loss to the point of being legally blindmay causevision loss to the point of being legally blind

the athlete to lose his vision partially and deteriorated over timecausedthe athlete to lose his vision partially and deteriorated over time

to a median survival of 6 months and an overall 5-year survival of < 5 % ( 3leadingto a median survival of 6 months and an overall 5-year survival of < 5 % ( 3

some of the symptoms such as vertigo and headaches and balance issuescausessome of the symptoms such as vertigo and headaches and balance issues

a progressive loss of vision as a result of damage to the central part of the retinacausesa progressive loss of vision as a result of damage to the central part of the retina

inflammation of the lining and wall of the large and/or small intestinecausesinflammation of the lining and wall of the large and/or small intestine

in devastating vision loss , sometimes at an early agecan resultin devastating vision loss , sometimes at an early age

from systemic copper deficiency caused by the failure of ATP7A to translocate copper from the small intestine into the circulation for delivery to the rest of the bodyresultsfrom systemic copper deficiency caused by the failure of ATP7A to translocate copper from the small intestine into the circulation for delivery to the rest of the body

vertigo and last weekcausesvertigo and last week

inflammation of blood vessels in the arteries , especially the coronary arteriescan causeinflammation of blood vessels in the arteries , especially the coronary arteries

a broad range of symptomscan causea broad range of symptoms

severe flu - like symptomscan causesevere flu - like symptoms

in faster of vitamin A form dimers and then lipofuscin accumulation of and the early start of visual symptoms , about regulatory blindness in nearly all cases What doresultingin faster of vitamin A form dimers and then lipofuscin accumulation of and the early start of visual symptoms , about regulatory blindness in nearly all cases What do

vision loss during childhood , adolescence and … Cataract surgery recovery is usually short and uneventful though there are symptoms which are common after surgerycausesvision loss during childhood , adolescence and … Cataract surgery recovery is usually short and uneventful though there are symptoms which are common after surgery

fungus with a 100 % mortality ratecausingfungus with a 100 % mortality rate

significant coral mortality worldwidecausessignificant coral mortality worldwide

the most decorated Winter Paralympian 's vision to declinecausedthe most decorated Winter Paralympian 's vision to decline

high mortality in newborn lambs and kidscauseshigh mortality in newborn lambs and kids

variant Esferocitosis relacionada con SPTB encausingvariant Esferocitosis relacionada con SPTB en

juvenile blindness — the U.S. Food and Drug Administration ( FDA ) has cleared the company 's Investigational New Drug ( IND ) applicationcausesjuvenile blindness — the U.S. Food and Drug Administration ( FDA ) has cleared the company 's Investigational New Drug ( IND ) application

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