WormMine

WS296

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0060671 cerebral cavernous malformation 3 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A cerebral cavernous malformation that has_material_basis_in mutation in the PDCD10 gene on chromosome 3q26.1.

1 Ontology

Name
Disease Ontology

10 Parents

Identifier Name Description
DOID:178 vascular disease A cardiovascular system disease that primarily affects the blood vessels which includes the arteries, veins and capillaries that carry blood to and from the heart.
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:863 nervous system disease A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
DOID:936 brain disease A central nervous system disease that is located_in the brain.
DOID:331 central nervous system disease A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system.
DOID:6713 cerebrovascular disease An vascular disease that is characterized by dysfunction of the blood vessels supplying the brain.
DOID:0060669 cerebral cavernous malformation A cerebrovascular disease that is characterized by dilated blood-filled capillaries lacking structural support.
DOID:0060671 cerebral cavernous malformation 3 A cerebral cavernous malformation that has_material_basis_in mutation in the PDCD10 gene on chromosome 3q26.1.

9 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0060669 DOID:0060671
is_a DOID:936 DOID:0060671
is_a DOID:1287 DOID:0060671
is_a DOID:7 DOID:0060671
is_a DOID:4 DOID:0060671
is_a DOID:331 DOID:0060671
is_a DOID:178 DOID:0060671
is_a DOID:863 DOID:0060671
is_a DOID:6713 DOID:0060671

0 Synonyms