Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Hereditary vascular disease

This group covers vascular (arterial, venous, and lymphatic ) damages clustered in families.

Systematic

Hereditary diseases
Hereditary broncho-pulmonary disease
Hereditary cardiac disease
Hereditary dermatological disorders
Hereditary diseases of the hematopoetic system and coagulopathies
Hereditary endocrinological diseases
Hereditary immunological disorders
Hereditary kidney diseases
Hereditary liver disease
Hereditary malformations
Hereditary metabolic diseases
Hereditary musculoskeletal diseases
Hereditary neurological disorders
Hereditary ocular disease and visual impairment
Hereditary otorhinolaryngological disorders
Hereditary pancreatic disease
Hereditary susceptibility to infections
Hereditary tumors
Hereditary vascular disease
Arteriosclerosis
APOB
APOE
HABP2
LDLR
LPA
MTHFR
PON1
SLC3A1
Diabetic microangiopathy 4
IL1RN
Generalized arterial calcification of infancy
Generalized arterial calcification of infancy 1
ENPP1
Generalized arterial calcification of infancy 2
ABCC6
Hereditary Angioedema
Hereditary Angioedema 1
SERPING1
Hereditary Angioedema 2
SERPING1
Hereditary Angioedema 3
F12
Hereditary lymphedema
Emberger syndrome
GATA2
Hennekam syndrome
Hennekam lymphangiectasia-lymphedema syndrome 1
CCBE1
Hennekam lymphangiectasia-lymphedema syndrome 2
FAT4
Hennekam lymphangiectasia-lymphedema syndrome 3
ADAMTS3
Hereditary lymphedema type 1a
FLT4
Hereditary lymphedema type 1c
GJC2
Hereditary lymphedema type 1d
VEGFC
Hereditary lymphedema with distichiasis
FOXC2
Hereditary lymphedema with distichiasis, diabetes, and renal involvement
FOXC2
Microcephaly-lymphedema-chorioretinopathy syndrome
KIF11
STING-associated vasculopathy with onset in infancy
TMEM173
Sneddon syndrome
ADA2
Susceptibility to arteriovenous malformations of the brain
IL6
Thromboembolic diseases
Autosomal dominant protein C deficiency
PROC
Autosomal dominant protein S deficiency
PROS1
Autosomal recessive protein C deficiency
PROC
Autosomal recessive protein S deficiency
PROS1
F2
F5
Factor XII deficiency
F12
HABP2
Hyperhomocysteinemic thrombosis
CBS
Hypoplasminogenemia
Dysplasminogenemia
PLG
Hypoplasminogenemia
PLG
MTHFR
PAI transcription modulator
SERPINE1
Protein Z deficiency
PROZ
SERPINA10
SERPINC1
THBD
Thrombophilia due to heparin cofactor 2 deficiency
SERPIND1
VKORC1
Vasculitis due to ADA2 deficiency
ADA2
Hypertension

References:

1.

Nguyen T et al. () Variability of response to clopidogrel: possible mechanisms and clinical implications.

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2.

Zambon A et al. (2006) Genetics of apolipoprotein B and apolipoprotein AI and premature coronary artery disease.

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3.

None (2006) Contribution of angiogenic genes to the complex genetic trait underlying Kawasaki disease.

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4.

None (2006) The genetics of heart attack.

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5.

Nordlie MA et al. (2006) Molecular aspects of ischemic heart disease: ischemia/reperfusion-induced genetic changes and potential applications of gene and RNA interference therapy.

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6.

Krischek B et al. (2006) The genetics of intracranial aneurysms.

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7.

None (2006) The molecular biology of thrombotic microangiopathy.

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8.

Szolnoki Z et al. (2006) Gene-gene and gene-environment interplay represent specific susceptibility for different types of ischaemic stroke and leukoaraiosis.

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9.

None (2006) Potential new risk factors for ischemic stroke: what is their potential?

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10.

Kim SH et al. (2006) Genetic mechanism of aspirin-induced urticaria/angioedema.

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11.

Orlacchio A et al. () Research actuality in the genetics of stroke.

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12.

Weiler CR et al. (2006) Genetic test indications and interpretations in patients with hereditary angioedema.

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13.

Bhoday J et al. (2006) The molecular mechanisms of vascular restenosis: Which genes are crucial?

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14.

Dashti SR et al. (2006) Molecular genetics of familial cerebral cavernous malformations.

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15.

Mahr AD et al. () Epidemiology of Wegener's granulomatosis: Lessons from descriptive studies and analyses of genetic and environmental risk determinants.

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16.

None (2006) The interaction between pathogens and the host coagulation system.

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17.

Uhlmann K et al. (2006) Genetics of diabetic retinopathy.

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Update: May 7, 2019