Pulmonary Venoocclusive Disease 1, Autosomal Dominant (PVOD1)

Alias:
Pulmonary Venoocclusive Disease 1
Pulmonary Veno-Occlusive Disease
Pvod1
Pvod
Pulmonary Veno-Occlusive Disease, Type 1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pulmonary Venoocclusive Disease 1, Autosomal Dominant, also known as pulmonary venoocclusive disease 1, is related to pulmonary venoocclusive disease and heritable pulmonary arterial hypertension, and has symptoms including hemoptysis An important gene associated with Pulmonary Venoocclusive Disease 1, Autosomal Dominant is BMPR2 (Bone Morphogenetic Protein Receptor Type 2). The drugs Bevacizumab and Orange have been mentioned in the context of this disorder. Affiliated tissues include lymph node and lung, and related phenotypes are centrilobular ground-glass opacification on pulmonary hrct and abnormally loud pulmonic component of the second heart sound
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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2
15
8

Medical Symptom

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

Gene & Mutation

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Mutations
No data available

Related Drugs

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CAS Number
Status
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No data available

Disease Model

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

References Literature

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PMID
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IF
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