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Disease core ontology applied to Rare Diseases
Last uploaded:
February 7, 2014
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| Preferred Name | Neuronal ceroid lipofuscinosis | |
| Synonyms |
NCL |
|
| ID |
http://www.limics.org/hrdo/rdfns#pat_id_650 |
|
| ageOfDeath |
Any age
|
|
| ageOfOnset |
Variable
|
|
| altLabel |
NCL
|
|
| id_Medline | ||
| id_MeSH |
D009472
|
|
| id_OMS |
E75.4
|
|
| id_Orpha |
216
|
|
| id_SNOMEDCT |
42012007
|
|
| id_UMLS |
C0027877
|
|
| inheritance |
Autosomal dominant Autosomal recessive
|
|
| patType |
group of phenomes
|
|
| prefixIRI |
hrdo:pat_id_650
|
|
| prefLabel |
Neuronal ceroid lipofuscinosis
|
|
| prevalence |
Unknown
|
|
| subClassOf |
http://www.limics.org/hrdo/rdfns#pat_id_18204 http://www.limics.org/hrdo/rdfns#pat_id_18253 http://www.limics.org/hrdo/rdfns#pat_id_11233 http://www.limics.org/hrdo/rdfns#pat_id_13730 http://www.limics.org/hrdo/rdfns#pat_id_13683 http://www.limics.org/hrdo/rdfns#pat_id_10525 |
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