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loading...| Preferred Name |
amyotrophic lateral sclerosis type 13 |
|
| Synonyms |
ALS13 |
|
| Definitions |
An association between 29 or more CAG repeats and the development of ALS13 exists. An amyotrophic lateral sclerosis where a mutation that has_material_basis_in the ATXN2 gene on chromosome 12 contributes to suscepitbility. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0060204 |
|
| comment |
An association between 29 or more CAG repeats and the development of ALS13 exists. |
|
| created by |
emitraka |
|
| creation_date |
2014-09-16T14:56:08Z |
|
| definition |
An amyotrophic lateral sclerosis where a mutation that has_material_basis_in the ATXN2 gene on chromosome 12 contributes to suscepitbility. |
|
| has exact synonym |
ALS13 amyotrophic lateral sclerosis 13 |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:0060204 |
|
| label |
amyotrophic lateral sclerosis type 13 |
|
| notation |
DOID:0060204 |
|
| prefLabel |
amyotrophic lateral sclerosis type 13 |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/DOID_0060204 | DOID | SAME_URI | |
| http://purl.obolibrary.org/obo/DOID_0060204 | HHEAR | SAME_URI | |
| http://purl.obolibrary.org/obo/DOID_0060204 | MIDO | SAME_URI | |
| http://purl.obolibrary.org/obo/DOID_0060204 | FNS-H | SAME_URI | |
| http://purl.obolibrary.org/obo/DOID_0060204 | HHEAR | LOOM | |
| http://purl.obolibrary.org/obo/DOID_0060204 | MIDO | LOOM | |
| http://purl.obolibrary.org/obo/DOID_0060204 | FNS-H | LOOM | |
| http://purl.obolibrary.org/obo/DOID_0060204 | DOID | LOOM |