Preferred Name |
optic atrophy 4 |
Synonyms |
OPA4 |
Definitions |
An optic atrophy that has_material_basis_in heterozygous mutation in a region on chromosome 18q12.2-q12.3. |
ID |
http://purl.obolibrary.org/obo/DOID_0111440 |
database_cross_reference |
OMIM:605293 MESH:C565343 |
definition |
An optic atrophy that has_material_basis_in heterozygous mutation in a region on chromosome 18q12.2-q12.3. |
has exact synonym |
OPA4 |
has material basis in | |
has_obo_namespace |
disease_ontology |
id |
DOID:0111440 |
label |
optic atrophy 4 |
notation |
DOID:0111440 |
prefLabel |
optic atrophy 4 |
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/OMIM/605293 | Online Mendelian Inheritance in Man | LOOM | |
http://purl.bioontology.org/ontology/MESH/C565343 | Medical Subject Headings | LOOM |