Loading ...
changes ( mutations ) in the GJA1 gene(passive) is caused byOculodentodigital dysplasia
A novel GJA1 mutationcausesoculodentodigital dysplasia
GJA1 ) mutationcausesoculodentodigital dysplasia
by a development arrest at the junction of the lateral side of the nose and the maxilla , which results in a complete or non - complete cleft between the nose and the orbital floor ( nasoocular cleft ) or between the mouth , nose and the orbital floor ( oronasal - ocular cleft(passive) is caused byNasomaxillary dysplasia
a development arrest at the junction of the lateral side of the nose and the maxilla , which results in a complete or non - complete cleft between the nose and the orbital floor ( nasoocular cleft ) or between the mouth , nose and the orbital floor ( oronasal - ocular cleft(passive) is caused byNasomaxillary dysplasia
Mutations in the FGFR3 genecausethanatophoric dysplasia
mutations in the SOX9 gene(passive) is caused byCampomelic dysplasia
a chromosomal mutation of the FGFR3 gene(passive) is caused byThanatophoric dysplasia
Mutations in the COL2A1 genecauseKniest dysplasia
by new mutations in the COL2A1 gene(passive) is caused byKniest dysplasia
by new mutations in the COL2A1 gene(passive) is causedKniest dysplasia
new mutations in the COL2A1 gene(passive) is caused byKniest dysplasia
FGFR3 mutationscausingthanatophoric dysplasia
by mutations in the RMRP gene(passive) can be caused byAnauxetic dysplasia
mutations in the RMRP gene(passive) can be caused byAnauxetic dysplasia
double missense FGFR3 mutations(passive) caused byThanatophoric dysplasia
by novel deletion mutations in the EDA gene(passive) caused bydysplasia
gene mutationscauseoculodentodigital dysplasia
mutations in the gene for Fibroblast growth factor receptor 3(passive) are caused bythanatophoric dysplasia
The mutationscausingthanatophoric dysplasia
by heterozygous mutations in Sox9(passive) is caused bycampomelic dysplasia
the SOX9 genecausescampomelic dysplasia
mutationscausingcampomelic dysplasia
by a large deletion mutation in the EDA gene(passive) caused bydysplasia
by a SOX9 mutation(passive) caused byCampomelic dysplasia
by a deletion upstream of the SOX9 gene(passive) caused bycampomelic dysplasia
dysplasia and two of whichcausethanatophoric dysplasia
by mutations of the p63 gene(passive) caused bydysplasia
mutations of the p63 gene(passive) caused bydysplasia
a development arrest before the union of the both nasal halves(passive) is caused byInternasal dysplasia
specific mutations in certain genes(passive) is caused bydysplasia
A mutant form of Connexin 43causesOculodentodigital dysplasia
Mutations in the IFT122 genecan causecranioectodermal dysplasia
infection(passive) are caused bycampomelic dysplasia
by abnormal joint development(passive) caused bydysplasia
the FBN1 mutations(passive) caused byzonular dysplasia
by the FBN1 mutations(passive) caused byzonular dysplasia
by HPV types 16 and 18(passive) caused bydysplasia
mutations in a connexin gene , GJB6 or connexin-30(passive) is caused bydysplasia
by premature(passive) caused bybronchopulmonary dysplasia
more severe bone abnormalities and very short stature , distinct facial features , abnormalities of the teeth , and mild intellectual disabilitycausesmore severe bone abnormalities and very short stature , distinct facial features , abnormalities of the teeth , and mild intellectual disability
renal artery stenosis(passive) caused byrenal artery stenosis
renal artery stenosiscausingrenal artery stenosis
most patients with renal artery stenosis(passive) caused bymost patients with renal artery stenosis
Focal renal artery stenosis(passive) caused byFocal renal artery stenosis
renal artery aneurysmsobviously can causerenal artery aneurysms
stenosis(passive) caused bystenosis
Efficacy of Revascularization For Renal Artery Stenosis(passive) Caused byEfficacy of Revascularization For Renal Artery Stenosis
stenosis of the renal artery , and therefore secondary hyperaldosteronismmay causestenosis of the renal artery , and therefore secondary hyperaldosteronism
your arteries to form abnormally creating areas of narrowing or stenosiscausesyour arteries to form abnormally creating areas of narrowing or stenosis
a number of complications , such as high blood pressure or tears of the artery ( dissectioncan causea number of complications , such as high blood pressure or tears of the artery ( dissection
renovascular hypertensioncausingrenovascular hypertension
the kidneys(passive) caused bythe kidneys
tearscan causetears
( Causecauses ( Cause
to an increased risk for aneurysmcan leadto an increased risk for aneurysm
a variety of other problems , including a kidney condition called nephronophthisis and eye abnormalitiescan also causea variety of other problems , including a kidney condition called nephronophthisis and eye abnormalities
my stroke(passive) was causedmy stroke
a beadingcausesa beading
to narrowing of major arteries ... usually in womenleadsto narrowing of major arteries ... usually in women
any symptomsmay ... causeany symptoms
a number of complicationscan causea number of complications
high blood pressure , a stroke and tears in other blood vesselscan also causehigh blood pressure , a stroke and tears in other blood vessels
most commonlycausesmost commonly
a number of complications , such as high blood pressure and aneurysmscan causea number of complications , such as high blood pressure and aneurysms
to RASleadingto RAS
RAScausingRAS
axis(passive) caused byaxis
abnormal cells growth in artery wallscausesabnormal cells growth in artery walls
hypertension , heart attacks , strokes , and arterial swellingcan causehypertension , heart attacks , strokes , and arterial swelling
high blood pressure , kidney failure , stroke and other symptomscan causehigh blood pressure , kidney failure , stroke and other symptoms
to severe leakage of the affected valvemay leadto severe leakage of the affected valve
alsocausesalso
Type I and II(passive) are causedType I and II
from a heterozygous missense mutation ( L113P ) in GJA1 ( connexin 43resultingfrom a heterozygous missense mutation ( L113P ) in GJA1 ( connexin 43
to hip instability , labral damage and early - onset arthritiscan leadto hip instability , labral damage and early - onset arthritis
to hip instability , labral damage , and early - onset arthritiscan leadto hip instability , labral damage , and early - onset arthritis
multiple developmental abnormalitiescausingmultiple developmental abnormalities
in the perinatal periodoriginatingin the perinatal period
in the perinatal period originatingin the perinatal period