Difference between revisions of "Hereditary Central Nervous System Demyelinating Diseases (disease - MeSH descriptor) (Q11052)"
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(Created claim: instance of (P17): Disease (Q8296)) |
(Removed [en] alias: D020279) |
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| (3 intermediate revisions by the same user not shown) | |||
| label / en | label / en | ||
| - | + | Hereditary Central Nervous System Demyelinating Diseases (disease - MeSH descriptor) | |
| aliases / en / 0 | aliases / en / 0 | ||
| + | MeSH:D020279 | ||
| aliases / en / 1 | aliases / en / 1 | ||
| - | |||
| Property / MeSH ID | |||
| + | |||
| Property / MeSH ID: D020279 / rank | |||
| + | Normal rank | ||
Latest revision as of 22:49, 20 October 2020
No description defined
- MeSH:D020279
| Language | Label | Description | Also known as |
|---|---|---|---|
| English |
Hereditary Central Nervous System Demyelinating Diseases (disease - MeSH descriptor)
|
No description defined
|
|
