CLN1 disease
http://www.orpha.net/ORDO/Orphanet_228329
Term info
database cross reference
- ICD-10:E75.4 (NTBT (narrower term maps to a broader term))
- UMLS:C1850451 (E (exact mapping (the terms and the concepts are equivalent)))
- ICD-10:E75.4 (Attributed)
- OMIM:256730 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref
UMLS:C1850451, ICD-10:E75.4, OMIM:256730
notation
ORPHA:228329
Term relations
Subclass of:
- etiological subtype
- has_annual_incidence_range some 1-9 / 100 000 and present_in some Finland and has_annual_incidence_average_value value 5.0
- has_inheritance some autosomal recessive
- part_of some Late infantile neuronal ceroid lipofuscinosis
- part_of some Infantile neuronal ceroid lipofuscinosis
- part_of some Juvenile neuronal ceroid lipofuscinosis
- has_age_of_onset some all ages
- part_of some Adult neuronal ceroid lipofuscinosis