Hereditary pulmonary embolism

In connection with hereditary thromboembolic disorders, pulmonary embolism occurs and pulmonary hypertension develops.

Systematic

Hereditary broncho-pulmonary disease
	Bronchiectasis with or without elevated sweat chloride
	Cystinosis
	Fabry disease
	Hereditary pulmonary embolism
		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
	Pulmonary alveolar microlithiasis
	Reduced response to beta-2-adrenoreceptor agonist
	Susceptibility to nocturnal asthma

References:

1.	Kominami S et al. (2009) HLA-DPB1 and NFKBIL1 may confer the susceptibility to chronic thromboembolic pulmonary hypertension in the absence of deep vein thrombosis.

2.	OMIM.ORG article Omim 612862

Update: Aug. 14, 2020

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