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by mutations in(passive) caused byapoptosis ( XIAP ) deficiency
by mutations in BIRC4(passive) caused byapoptosis ( XIAP ) deficiency
Drugscausehemolysis ( G6PD deficiency
by the dysfunction of hypothalamic - pituitary - adrenal axis(passive) caused byGlucocorticoid secretion deficiency
Novel mutations in the CYP11B2 genecausingaldosterone synthase deficiency
by a novel mutation in the MTCO1 gene(passive) caused bycytochrome c oxidase deficiency
a novel mutation in the MTCO1 gene(passive) caused bycytochrome c oxidase deficiency
Loss of mtDNA ... loss of mtDNAcausedcytochrome C oxidase deficiency
some gram - negative leukotriene receptor blockers(passive) can be caused byAciclovir monophosphate dehydrogenase deficiency
mutations in the DPYD gene(passive) is caused byDihydropyrimidine dehydrogenase deficiency
the genetic defectcausingglucose-6-phosphate dehydrogenase deficiency ( G6PD
by SURF1 gene m(passive) caused bycytochrome c oxidase deficiency
by mutation in SURF1(passive) caused byCytochrome - c oxidase deficiency
a loss of nicotinic receptors in the brainresultingacetylcholine deficiency
recessive and dominant mutations(passive) is caused byMethionine adenosyltransferase deficiency
by homozygous SURF1 mutation(passive) caused bycytochrome c oxidase deficiency
Stratumcausescorneum ceramide deficiency
by hypothalamic lesions(passive) caused byHypothalamic ACTH deficiency
pituitary disease or suppression of the hypothalamic - pituitary axis(passive) may be caused byACTH deficiency
Any disorder of the pituitary or hypothalamuscan causeACTH deficiency
the genetic defect ... , which is characterised by reduced NADPH levelscausingglucose-6-phosphate dehydrogenase deficiency ( G6PD
Any cause of pituitary diseasemay causeACTH deficiency
by adrenal insufficiency(passive) caused byACTH deficiency
mutations in the G6PD gene(passive) is caused bydehydrogenase deficiency
Caffeinecan causeinositol deficiency
mutation in the G6PD gene(passive) is caused byG6PD deficiency
Underactive pituitary glandmay causeACTH deficiency
the diseasesmay causeACTH deficiency
the factorscan causea deficiency in diamine oxidase
an alteration ( a mutation or a change ) in the G6PD gene(passive) is caused byG6PD deficiency
MOCS1 or MOCS2(passive) caused bySulfite oxidase deficiency
vitamin B4 deficiency , which natural shilajit replenishes(passive) is caused byAcetylcholine deficiency
different mutations(passive) caused byG6PD deficiency
by compound heterozygosity for two novel mutations in the TCN2 gene(passive) caused byTranscobalamin deficiency
compound heterozygosity for two novel mutations in the TCN2 gene(passive) caused byTranscobalamin deficiency
More than 20 mutations in the TCN2 gene have been foundto causetranscobalamin deficiency
Niacinleadsnicotinamide - deficiency
by compound heterozygosity(passive) caused byTranscobalamin deficiency
autosomal recessive neonatal cholestasis(passive) caused byautosomal recessive neonatal cholestasis
to mental retardation and excretion of cysteine in the urineleadsto mental retardation and excretion of cysteine in the urine
to excretion of HGA in urineleadingto excretion of HGA in urine
to excretion of HGAleadingto excretion of HGA
variegate porphyriacausesvariegate porphyria
variegatecausesvariegate
to AD pathogenesismay contributeto AD pathogenesis
a form of Leigh Syndromecausesa form of Leigh Syndrome
in hemolysis of red blood cells followingcan resultin hemolysis of red blood cells following
hereditarycauseshereditary
hereditary coproporphyriacauseshereditary coproporphyria
histamine intolerancemay causehistamine intolerance
the rare genetic disorder - Xanthinuriacausesthe rare genetic disorder - Xanthinuria
variegatecausesvariegate
variegate porphyriacausesvariegate porphyria
to muscle weakness ( myopathy ) , poor muscle tone ( hypotonia ) , severe brain dysfunction ( encephalomyopathycan leadto muscle weakness ( myopathy ) , poor muscle tone ( hypotonia ) , severe brain dysfunction ( encephalomyopathy
anaemiacausesanaemia
to liver inflammation , anemia , and premature graying of haircan leadto liver inflammation , anemia , and premature graying of hair
cochlear innervation abnormalities in micecausescochlear innervation abnormalities in mice
in reduced growth and feed efficiencyresultedin reduced growth and feed efficiency
in mental retardation and excretion of cysteine in the urineresultsin mental retardation and excretion of cysteine in the urine
to fatty degenerationmay leadto fatty degeneration
loss of pigmentationmay causeloss of pigmentation
protein synthesis in the bodycan causeprotein synthesis in the body
gray haircausesgray hair
hearing loss(passive) may ... be caused byhearing loss
to fatty liverleadingto fatty liver
hypomethylation of DNAcauseshypomethylation of DNA
to cognitive problems , dementia and cardiovascular diseasecan leadto cognitive problems , dementia and cardiovascular disease
A. Pyridoxine - Dependent Epilepsy in Zebrafish(passive) Caused byA. Pyridoxine - Dependent Epilepsy in Zebrafish
to edema ( retention of fluidcan leadto edema ( retention of fluid
dementia , apathy , edema , lethargycan causedementia , apathy , edema , lethargy
lysosomal dysfunction and oxidative stress in models of Snyder - Robinson syndromecauseslysosomal dysfunction and oxidative stress in models of Snyder - Robinson syndrome
in fatty liver , slow growth , weakness , edema and skin lesionsmay resultin fatty liver , slow growth , weakness , edema and skin lesions
in fatty liver , slow growth , weakness , edema and skin lesionsmay resultin fatty liver , slow growth , weakness , edema and skin lesions
to fatty liver : kwashiorkor , a disease affecting children with low protein intakeleadingto fatty liver : kwashiorkor , a disease affecting children with low protein intake
normal cystine content(passive) caused bynormal cystine content
the liver to metabolize only histidine , which results in an incomplete form of folic acidcausesthe liver to metabolize only histidine , which results in an incomplete form of folic acid
in acetyl - CoAresultsin acetyl - CoA
dementia , apathy , edema , lethargy , liver damage , muscle loss , weakness , slow growth and skin lesionscan causedementia , apathy , edema , lethargy , liver damage , muscle loss , weakness , slow growth and skin lesions