ceroid lipofuscinosis, neuronal, 1

Preferred Label : ceroid lipofuscinosis, neuronal, 1;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0565253;

UMLS CUI

C1850451;

Currated CISMeF NLP mapping
- Ceroid lipofuscinosis, neuronal, 1 [OMIM Phenotype]
- Infantile neuronal ceroid lipofuscinosis [ICD-11 More detail]
- Infantile neuronal ceroid lipofuscinosis [ORDO Disease]
- Infantile neuronal ceroid lipofuscinosis (disorder) [SNOMED CT concept]
- Neuronal Ceroid Lipofuscinosis Type 1 [NCIt concept]
- infantile neuronal ceroid lipofuscinosis [SNOMED Notion]
- infantile neuronal ceroid lipofuscinosis [Disease (Nov.)]
- neuronal ceroid lipofuscinosis 1 [DO Concept]
Related record
- ceroid lipofuscinosis, neuronal, 1 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CLN1 disease [ORDO Disease]
- Ceroid lipofuscinosis, neuronal, 1 [OMIM Phenotype]
Validated automatic mappings to BTNT
- CLN1 disease [ORDO Disease]