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Center for Nephrology and Metabolic Disorders
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Omim
Hereditary vascular disease
This group covers vascular (arterial, venous, and lymphatic ) damages clustered in families.
Systematic
Hereditary diseases
Genetic alterations of drug tolerance
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
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
Vascular calcification
Calciphylaxis
FGF23
NT5E
VDR
Generalized arterial calcification of infancy
Generalized arterial calcification of infancy 1
ENPP1
Generalized arterial calcification of infancy 2
ABCC6
Hereditary arterial and articular multiple calcification syndrome
NT5E
Vasculitis due to ADA2 deficiency
ADA2
Hypertension
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