WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0110073 arrhythmogenic right ventricular dysplasia 4 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.

1 Ontology

Name
Disease Ontology

13 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:1287 cardiovascular system disease A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis.
DOID:114 heart disease A cardiovascular system disease that involves the heart.
DOID:0060118 thoracic disease A disease of anatomical entity that is located_in the thoracic cavity.
DOID:0050177 monogenic disease A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.
DOID:0050736 autosomal dominant disease An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.
DOID:0050739 autosomal genetic disease A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.
DOID:0060036 intrinsic cardiomyopathy A cardiomyopathy that is characterized as weakness in the muscle of the heart that is not due to an identifiable external cause.
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy An intrinsic cardiomyopathy that is characterized by hypokinetic areas involving the free wall of the right ventricle, with fibrofatty replacement of the right ventricular myocardium, with associated arrhythmias originating in the right ventricle and limited or no involvement of the left ventricle.
DOID:0050700 cardiomyopathy A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.
DOID:0110073 arrhythmogenic right ventricular dysplasia 4 An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.

12 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050736 DOID:0110073
is_a DOID:0050431 DOID:0110073
is_a DOID:630 DOID:0110073
is_a DOID:0050177 DOID:0110073
is_a DOID:0060036 DOID:0110073
is_a DOID:0050700 DOID:0110073
is_a DOID:0060118 DOID:0110073
is_a DOID:0050739 DOID:0110073
is_a DOID:4 DOID:0110073
is_a DOID:7 DOID:0110073
is_a DOID:114 DOID:0110073
is_a DOID:1287 DOID:0110073

4 Synonyms

Name Type
arrhythmogenic right ventricular cardiomyopathy 4 synonym
ARVC4 synonym
ARVD4 synonym
familial arrhythmogenic right ventricular dysplasia 4 synonym