WormMine

WS296

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0050952 spastic ataxia Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A hereditary ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy.

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: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: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:1289 neurodegenerative disease A central nervous system disease that results in the progressive deterioration of function or structure of neurons.
DOID:0050951 hereditary ataxia A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
DOID:0050952 spastic ataxia A hereditary ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy.

13 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050952 DOID:0050772
is_a DOID:0050952 DOID:0050941
is_a DOID:0050952 DOID:0050942
is_a DOID:0050952 DOID:0050943
is_a DOID:0050952 DOID:0050944
is_a DOID:0050952 DOID:0050945
is_a DOID:0050951 DOID:0050952
is_a DOID:7 DOID:0050952
is_a DOID:863 DOID:0050952
is_a DOID:1289 DOID:0050952
is_a DOID:331 DOID:0050952
is_a DOID:4 DOID:0050952
is_a DOID:0050952 DOID:0080252

0 Synonyms