Heart Disease

Alias:
Heart Failure
Congenital Heart Disease
Congenital Heart Defects
Heart Diseases
Congenital Anomaly of Heart
Congenital Heart Anomalies
Disease, Heart, Congenital
Congenital Heart Disorder
Heart Defects, Congenital
Heart Disease, Congenital
Congestive Heart Failure
Heart Defects Congenital
Congenital Heart Defect
Heart-Congenital Defect
Heart Malformation
Heart Defects
Heart Defect
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Heart Disease, also known as heart failure, is related to heart valve disease and lipoprotein quantitative trait locus, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Heart Disease is NKX2-5 (NK2 Homeobox 5), and among its related pathways/superpathways are Human Embryonic Stem Cell Pluripotency and Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers. The drugs Verapamil and Hydrochlorothiazide have been mentioned in the context of this disorder. Affiliated tissues include heart and bone marrow.
Related ID:
MESH:D006330
ICD11:1458683894

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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Medical Symptom

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

Gene & Mutation

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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
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IF
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