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Neuronal ceroid lipofuscinosis
Adnoddau allanol
| WikiProjectMed ID | |
| dynodwr Microsoft Academic | |
| dynodwr MeSH | C537948[1]mapping relation type: exact match |
| Mondo ID | |
| dynodwr YSO | 581[2]enwyd fel: INCL-tauti, infantil neuronal ceroidlipofuscinos, infantile neuronal ceroid lipofuscinosis |
| dynodwr KEGG | |
| UMLS CUI | C0268281[1]mapping relation type: exact match C2931673[1]mapping relation type: exact match |
| ICD-11 (foundation) | |
| dynodwr OMIM | |
| Orphanet ID | 79263[1]mapping relation type: exact match |
| ICD-10-CM | |
| DiseasesDB | |
enghraifft o'r canlynol
clefyd prin
dosbarth o glefyd
isddosbarth o'r canlynol
neuronal ceroid lipofuscinosis[1] rhan o'r canlynol
Finnish heritage disease
Cyfeiriadau
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Monarch Disease Ontology release 2018-06-29, 3 Gorffennaf 2018, MONDO_0019261
- ↑ YSO-Wikidata mapping project, 2 Chwefror 2022
- ↑ 3.0 3.1 Mesh ID
