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heterozygous or homozygous mutation in the OPLAH gene ( 5-Oxoprolinase(passive) can be caused by5-oxoprolinase deficiency
by defects in ALAS1 protein production(passive) is ... caused byheme deficiency
by mutations in the collagen - like tail subunit ( ColQ ) of the asymmetric enzyme(passive) caused byacetylcholinesterase deficiency
Underactive pituitary glandmay causeACTH deficiency
mutationcausedheme deficiency
recessive mutations in the AAT gene(passive) is caused byAntitrypsin deficiency
The alas1 mutationcausedheme deficiency
by several types of porphyria(passive) caused byHeme deficiency
several types of porphyria(passive) caused byHeme deficiency
by a novel mutation ( p(passive) caused byantitrypsin deficiency
Pernicious anemiamay also causecobalamin deficiency
vitamin B12 deficiency ... pernicious anemiacan ... causecobalamin deficiency
compound heterozygosity for two novel mutations in the TCN2 gene(passive) caused byTranscobalamin deficiency
other disorders ... vitamin B12can causecobalamin deficiency
More than 20 mutations in the TCN2 gene have been foundto causetranscobalamin deficiency
at any age(passive) can be discoveredFibrinogen deficiency
either inadequate intake , inadequate absorption from food or malabsorption due to intestinal problems(passive) is caused byDeficiency
most often(passive) is ... causedCobalamin deficiency
inadequate supply to the body , improper absorption by the body of such nutrients or due to unable to maintain the content of zinc vitamins required by the body(passive) may be caused byDeficiency
Nitrous oxidecan causecobalamin deficiency
homozygous or compound heterozygous mutations in DOCK8 gene(passive) is caused byDOCK8 deficiency
Nitrous Oxide Exposure to nitrous oxidecausescobalamin deficiency
by a nonsense mutation and an A - to - G splice site mutation at position(passive) caused byacetylcholinesterase deficiency
B. Folate and/orcan causecobalamin deficiency
the factor that sometimes it is not absorbed properly , ... : It is generally not the lack of B12 in our diet that leads to a functional decrease in B12 levelscausesdeficiency
lack of B12 in the diet , pernicious anemia or impaired absorption by the intestines(passive) can be caused byDeficiency
an autoimmune processcauseshypocretin - deficiency
by celiac disease(passive) caused byCholecystokinin deficiency
inadequate exposure to sunlight and low consumption of foods containing Vitamin D.(passive) is caused byDeficiency
complete deficiency of the protein DOCK8(passive) is caused byDOCK8 deficiency
inadequate dietary intake of the vitamin , malabsorption , metabolic abnormalities , or drug - nutrient interactions(passive) is caused byDeficiency
lack of exposure to sunlight , dietary deficiency or malabsorption(passive) is caused by Deficiency
low dietary intake , malabsorption and increased excretion due to common illnesses(passive) is caused byDeficiency
disease , drug use , reduced digestive function , or inadequate magnesium intake(passive) may be caused byDeficiency
not by a lack of B-12 in the diet , but rather impaired absorption(passive) is often causedDeficiency
by disease and syndrome of spleen deficiency syndrome(passive) caused bydeficiency
For the body to absorb vitamin b12 better there is a requirement of a protein called intrinsic factor , lack of this proteintoo can causedeficiency
a lack of intrinsic factor - the substance needed for the absorption of vitamin B12(passive) is also caused byDeficiency
a prolonged vegan diet without supplementation , alcoholism(passive) can be caused byDeficiency
inadequate dietary intake of the vitamin , malabsorption , or metabolic abnormalities(passive) is caused byDeficiency
to RAS activationleadsto RAS activation
narcolepsy may causenarcolepsy
narcolepsy may causenarcolepsy
the narcolepsycausesthe narcolepsy
narcolepsycausesnarcolepsy
narcolepsymay causenarcolepsy
Narcolepsy with cataplexy(passive) is caused byNarcolepsy with cataplexy
developmental defects in the substantia nigra(passive) caused bydevelopmental defects in the substantia nigra
to hyperactive Ras - MAPK signalingleadsto hyperactive Ras - MAPK signaling
to folate deficiency , which , in turn , increases homocysteine levels and may result in the development of cardiovascular disease or birth defectsmay leadto folate deficiency , which , in turn , increases homocysteine levels and may result in the development of cardiovascular disease or birth defects
to megaloblastic anemialeadsto megaloblastic anemia
to the loss of heme - related granule protein activities , defective granule formationledto the loss of heme - related granule protein activities , defective granule formation
to the loss of heme - related granule protein activities , defective granule formation , andledto the loss of heme - related granule protein activities , defective granule formation , and
apoptosiscausesapoptosis
serious diseases in humans , such as anemia , porphyrias , and Alzheimer 's diseasecan causeserious diseases in humans , such as anemia , porphyrias , and Alzheimer 's disease
alsoleadsalso
to the loss of heme - related granule protein activities , defective granule formation , and altered immune responses against pathogenic bacterialedto the loss of heme - related granule protein activities , defective granule formation , and altered immune responses against pathogenic bacteria
megaloblastic anemia and neurocognitive abnormalities but effects on immune function and bone formation have also been describedcausesmegaloblastic anemia and neurocognitive abnormalities but effects on immune function and bone formation have also been described
in pernicious anaemia ... i.e. decreased number of erythrocytes in bone marrowresultsin pernicious anaemia ... i.e. decreased number of erythrocytes in bone marrow
in hypoxic ( low - oxygen ) cellular conditionsresultsin hypoxic ( low - oxygen ) cellular conditions
decreased function of the monoaminergic system , which leads to low levels of serotonin and norepinephrinecausesdecreased function of the monoaminergic system , which leads to low levels of serotonin and norepinephrine
a reversible dementia in elderly patientsmay causea reversible dementia in elderly patients
to itching , dry scalpleadsto itching , dry scalp
to the apoptosis - independent depletion of the lens epithelial cell layeralso ledto the apoptosis - independent depletion of the lens epithelial cell layer
to neurodegeneration and impaired neuronal migrationleadsto neurodegeneration and impaired neuronal migration
subdermal lipodystrophy and resistancecausessubdermal lipodystrophy and resistance
to ADHD phenotypesleadsto ADHD phenotypes
to profound congenital hearing lossleadsto profound congenital hearing loss
to an alteration in the basal metabolic rate mediated through the autonomic nervous systemleadsto an alteration in the basal metabolic rate mediated through the autonomic nervous system
problems with falling asleepcan causeproblems with falling asleep
Ras - mediated granulocyte / macrophage colony stimulating factor hypersensitivity and chronic myeloidcausesRas - mediated granulocyte / macrophage colony stimulating factor hypersensitivity and chronic myeloid
A combined immunodeficiency with severe infections , inflammation and allergy(passive) caused byA combined immunodeficiency with severe infections , inflammation and allergy
in elevated glutamatecan resultin elevated glutamate
Combined immunodeficiency with severe inflammation and allergy(passive) caused byCombined immunodeficiency with severe inflammation and allergy
Ras - mediated granulocyte - macrophage colony stimulating factor hypersensitivity and chronic myeloid leukemiacausesRas - mediated granulocyte - macrophage colony stimulating factor hypersensitivity and chronic myeloid leukemia
Ras - mediated granulocyte / macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemiacausesRas - mediated granulocyte / macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia
Ras - mediated granulocyte / macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemiacausesRas - mediated granulocyte / macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia
to ADHD phenotypes and that impaired astroglial glutamate clearance , a mechanism distinct from the well - established dopamine deficit hypothesis for ADHD , underlies the resultant behavioral abnormalitiesleadsto ADHD phenotypes and that impaired astroglial glutamate clearance , a mechanism distinct from the well - established dopamine deficit hypothesis for ADHD , underlies the resultant behavioral abnormalities
a general effect on mRNA translation ... or whether it results in aberrant translation of specific mRNAs that contributes to the SDS phenotypecausesa general effect on mRNA translation ... or whether it results in aberrant translation of specific mRNAs that contributes to the SDS phenotype
in progressive loss of lens epithelial cells and the loss of both histone H1 and lamin A / C phosphorylation in lens fiber cell nucleiresultedin progressive loss of lens epithelial cells and the loss of both histone H1 and lamin A / C phosphorylation in lens fiber cell nuclei