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Qaagi - Book of Why

Causes

Effects

mutations in the LPIN2 gene(passive) is caused byMajeed syndrome

by mutations in LPIN2(passive) is caused byMajeed syndrome

by mutations in LPIN2(passive) caused byMajeed syndrome

the increased secretion of immunoglobulin by a monoclonal line of immunoglobulin producing cells(passive) is caused byHyperviscosity syndrome

the disease ... the mutated genescauseMajeed Syndrome

Waldenstrom macroglobulinemia(passive) caused byhyperviscosity syndrome

until the level of cryoglobulinemia is sufficiently highto causehyperviscosity syndrome

The reason why monoclonal gammopathy is bad iscan causehyperviscosity syndrome

the severe blood loss(passive) is caused bySheehan?s Syndrome

changes or mutations in the JAG1 and NOTCH2 genes(passive) is caused byAlagille syndrome

mutations or defects in the JAG1 and NOTCH2 genes(passive) is caused byAlagille syndrome

severe blood loss during or after childbirth(passive) is caused bySheehan?s Syndrome

by mutations in the NOTCH2 gene(passive) caused byAlagille syndrome

severe blood loss or extremely low blood pressure during or after childbirth(passive) is caused bySheehan?s syndrome

mutations human Jagged1 , which encodes a ligand for Notch 1(passive) is caused byAlagille syndrome

mutations in human Jagged1 , which encodes a ligand for Notch1(passive) is caused byAlagille syndrome

changes , or mutations(passive) is caused byAlagille syndrome

The Jag1 mutations associated withleadAlagille syndrome

mutations in JAGGED1 or NOTCH2(passive) is caused byAlagille syndrome

mutations in JAG1 ( seen in 94 % ) and NOTCH2 ( seen in 1 % ) genes(passive) is caused byAlagille syndrome

the genecausesAlagille syndrome

hereditary or spontaneous mutations in JAG1 or NOTCH2 on chromosome 20(passive) is caused byAlagille syndrome

by NOTCH2 mutation(passive) caused byAlagille syndrome

a gene transformation , or defect(passive) caused byAlagille syndrome

Mutations in NOTCH2 ... much less likelyto causeAlagille syndrome

Gene mutationscauseAlagille syndrome

mutations in any of several genes(passive) may be caused bySwyer syndrome

to be affectedto causeAlagille syndrome

A nonsense mutation in MSX1causesWitkop syndrome

cholestasis(passive) caused byAlagille syndrome

an abnormal chromosome(passive) caused bymyelodysplastic syndrome

a genetic defect that happens when there is a mutation ( permanent change ) in the DNA sequence of your child(passive) is caused byAlagille syndrome

defects in genes involved in the Notch signaling pathway(passive) is caused byAlagille syndrome

a gene mutation that can pass from parent to child(passive) is caused byAlagille syndrome

a mutation in the MSX1 gene located on chromosome 4p16(passive) is caused byWitkop syndrome

marijuanaDoes ... causeamotivational syndrome

Marijuanacausesamotivational syndrome

by cannabis use(passive) caused byamotivational syndrome

cannabis usecausesamotivational syndrome

exposure to harmful chemicals or radiation(passive) is caused bymyelodysplastic syndrome

in bleeding , headache , dizziness and hearing or visual problemsmay resultin bleeding , headache , dizziness and hearing or visual problems

neurologic symptoms , such as headache and visual changesmay causeneurologic symptoms , such as headache and visual changes

alsomay causealso

in hypertension and retinal hemorrhagescan ... resultin hypertension and retinal hemorrhages

in a poor response to chemotherapy , fatigue , and a reduced quality of life for cancer patientscan resultin a poor response to chemotherapy , fatigue , and a reduced quality of life for cancer patients

intellectual disabilitiescausesintellectual disabilities

symptoms including weakness , fatigue , joint pain and morecausessymptoms including weakness , fatigue , joint pain and more

the pituitary gland to not produce enough pituitary hormones ( hypopituitarismcausesthe pituitary gland to not produce enough pituitary hormones ( hypopituitarism

the poor wound healing(passive) caused bythe poor wound healing

the permanent underproduction of essential pituitary hormones ( hypopituitarismcausesthe permanent underproduction of essential pituitary hormones ( hypopituitarism

problems in the liver , heart , eyes , spine , and kidneyscausesproblems in the liver , heart , eyes , spine , and kidneys

the top of the femur Femur The femur , or thigh bonecausesthe top of the femur Femur The femur , or thigh bone

to clots that lead to strokes , heart attacks or other serious medical issuescould leadto clots that lead to strokes , heart attacks or other serious medical issues

chronic anemia , and anemia(passive) caused bychronic anemia , and anemia

to acute leukemiacould leadto acute leukemia

the topcausesthe top

to leukemialeadsto leukemia

to leukemiacan leadto leukemia

to the development of stretch markscan leadto the development of stretch marks

usuallycausesusually

ineffective production of blood cellscausesineffective production of blood cells

to complications that affect the liver and other parts of the bodycan leadto complications that affect the liver and other parts of the body

neutropeniacan causeneutropenia

bile duct abnormalities in the livercausesbile duct abnormalities in the liver

cells to be irregular shapescausescells to be irregular shapes

the top of the femur ( thigh bone ) to degenerate , occurs in Yorkies in certain linescausesthe top of the femur ( thigh bone ) to degenerate , occurs in Yorkies in certain lines

alsocan ... causealso

in livercan resultin liver

to acute myeloid leukemia ( AMLleadto acute myeloid leukemia ( AML

complications in other parts of the body , such asmay causecomplications in other parts of the body , such as

problems with the bile ductscausesproblems with the bile ducts

to heart problemscan eventually leadto heart problems

the liver damage(passive) caused bythe liver damage

to serious complicationscan leadto serious complications

progressive destruction of the bile ductscausesprogressive destruction of the bile ducts

from benzene exposureresultingfrom benzene exposure

from heterogeneous gene mutations , including mutations in JAG1 on CHROMOSOME 20may resultfrom heterogeneous gene mutations , including mutations in JAG1 on CHROMOSOME 20

narrowing ( stenosis ) or bulging ( aneurysm ) of other blood vessels in the bodycan also causenarrowing ( stenosis ) or bulging ( aneurysm ) of other blood vessels in the body

primary thrombocytosiscausesprimary thrombocytosis

to cirrhosis and portal hypertensionleadsto cirrhosis and portal hypertension

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