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

Update:

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