WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0111073 progressive familial heart block Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A heart conduction disease characterized by autosomal dominant inheritance of a cardiac conduction defect that may progress to complete atrioventricular (AV) block and maybe asymptomatic of manifest as shortness of breath, dizziness, syncope, abdominal pain, heart failure or sudden death.

1 Ontology

Name
Disease Ontology

7 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:10273 heart conduction disease A cardiovascular system disease that involves the heart's electrical conduction system.
DOID:0111073 progressive familial heart block A heart conduction disease characterized by autosomal dominant inheritance of a cardiac conduction defect that may progress to complete atrioventricular (AV) block and maybe asymptomatic of manifest as shortness of breath, dizziness, syncope, abdominal pain, heart failure or sudden death.

9 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:10273 DOID:0111073
is_a DOID:4 DOID:0111073
is_a DOID:1287 DOID:0111073
is_a DOID:0060118 DOID:0111073
is_a DOID:114 DOID:0111073
is_a DOID:7 DOID:0111073
is_a DOID:0111073 DOID:0111074
is_a DOID:0111073 DOID:0111075
is_a DOID:0111073 DOID:0111076

7 Synonyms

Name Type
familial Lenegre disease synonym
familial Lev disease synonym
familial Lev-Lenegre disease synonym
familial PCCD synonym
familial progressive heart block synonym
hereditary bundle branch defect synonym
PFHB synonym