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loading...| Preferred Name |
Mannosidase Deficiency Diseases [Disease/Finding] |
|
| Synonyms |
Mannosidase Deficiency Diseases Mannosidase Deficiency Syndromes |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000010936 |
|
| altLabel |
Mannosidase Deficiency Diseases Mannosidosis Mannosidase Deficiency Syndromes |
|
| cui |
C1257960 |
|
| MESH DEFINITION |
Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme. |
|
| MESH DUI |
D044904 |
|
| MeSH name |
Mannosidase Deficiency Diseases |
|
| MESH UI |
M0446510 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000010936 |
|
| NUI |
N0000010936 |
|
| prefLabel |
Mannosidase Deficiency Diseases [Disease/Finding] |
|
| SNOMED CID |
65524005 |
|
| tui |
T047 |
|
| subClassOf |
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