WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:13945 CADASIL Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.

1 Ontology

Name
Disease Ontology

8 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: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:10579 leukodystrophy A cerebral degeneration characterized by dysfunction of the white matter of the brain.
DOID:1443 cerebral degeneration A brain disease that is characterized by loss of structure or function of neurons, including death of neurons and loss of brain tissue.
DOID:13945 CADASIL A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.

9 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:13945 DOID:0111035
is_a DOID:13945 DOID:0111036
is_a DOID:10579 DOID:13945
is_a DOID:331 DOID:13945
is_a DOID:863 DOID:13945
is_a DOID:1443 DOID:13945
is_a DOID:7 DOID:13945
is_a DOID:4 DOID:13945
is_a DOID:936 DOID:13945

2 Synonyms

Name Type
cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy synonym
hereditary multi-infarct dementia synonym