WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0060868 leukoencephalopathy with vanishing white matter Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood.

1 Ontology

Name
Disease Ontology

12 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: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: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:0050737 autosomal recessive disease An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop.
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:0060868 leukoencephalopathy with vanishing white matter A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood.

16 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050737 DOID:0060868
is_a DOID:10579 DOID:0060868
is_a DOID:331 DOID:0060868
is_a DOID:630 DOID:0060868
is_a DOID:0050177 DOID:0060868
is_a DOID:863 DOID:0060868
is_a DOID:0050739 DOID:0060868
is_a DOID:1443 DOID:0060868
is_a DOID:7 DOID:0060868
is_a DOID:4 DOID:0060868
is_a DOID:936 DOID:0060868
is_a DOID:0060868 DOID:0070367
is_a DOID:0060868 DOID:0070371
is_a DOID:0060868 DOID:0070372
is_a DOID:0060868 DOID:0070373
is_a DOID:0060868 DOID:0070374

5 Synonyms

Name Type
ovarioleukodystrophy synonym
CACH synonym
CACH/VWM synonym
childhood ataxia with central nervous system hypomyelination synonym
vanishing white matter leukodystrophy synonym