Pulmonary Venoocclusive Disease (PVOD)

Alias:
Pulmonary Veno-Occlusive Disease
Pulmonary Venoocclusive Disease 1, Autosomal Dominant
Venous Form of Primary Pulmonary Hypertension
Obstructive Disease of the Pulmonary Veins
Isolated Pulmonary Venous Sclerosis
Pvod
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pulmonary Venoocclusive Disease, also known as pulmonary veno-occlusive disease, is related to pulmonary venoocclusive disease 1, autosomal dominant and telangiectasis, and has symptoms including hemoptysis An important gene associated with Pulmonary Venoocclusive Disease is EIF2AK4 (Eukaryotic Translation Initiation Factor 2 Alpha Kinase 4), and among its related pathways/superpathways are Signal Transduction and Human Embryonic Stem Cell Pluripotency. The drugs Bevacizumab and Orange have been mentioned in the context of this disorder. Affiliated tissues include lung and heart, and related phenotypes are Decreased substrate adherent cell growth and Increased human cytomegalovirus (HCMV) strain AD169 replication
Related ID:
MESH:D011668

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
<1/1000000
26
297
--

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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