WormMine

WS296

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0111443 optic atrophy 2 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  An optic atrophy that has_material_basis_in variation in a region on chromosome Xp11.4-p11.21.

1 Ontology

Name
Disease Ontology

9 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:574 peripheral nervous system disease A nervous system disease that affects the peripheral nervous system.
DOID:870 neuropathy A nervous system disease that is located_in nerves or nerve cells.
DOID:5656 cranial nerve disease A neuropathy that is located_in one of the twelve cranial nerves.
DOID:1891 optic nerve disease A cranial nerve disease that is located_in the optic nerve.
DOID:5723 optic atrophy An optic nerve disease that is characterized the death of the retinal ganglion cell axons that comprise the optic nerve.
DOID:0111443 optic atrophy 2 An optic atrophy that has_material_basis_in variation in a region on chromosome Xp11.4-p11.21.

8 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:5723 DOID:0111443
is_a DOID:5656 DOID:0111443
is_a DOID:870 DOID:0111443
is_a DOID:574 DOID:0111443
is_a DOID:7 DOID:0111443
is_a DOID:1891 DOID:0111443
is_a DOID:863 DOID:0111443
is_a DOID:4 DOID:0111443

2 Synonyms

Name Type
OPA2 synonym
X-linked optic atrophy 2 synonym