infantile neuronal ceroid lipofuscinosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0019261


Infantile neuronal ceroid lipofuscinosis (INCL) is a form of neuronal ceroid lipofuscinosis (NCL) characterized by onset during the second half of the first year of life and rapid mental and motor deterioration leading to loss of all psychomotor abilities. [ Orphanet:79263 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:79263 (MONDO:equivalentTo)
  • SCTID:58258004 (MONDO:equivalentTo)
  • ICD10:E75.4 (Orphanet:79263)
Subsets

ordo_disease

abbreviation
INCL [ Orphanet:79263 ]

definition

Infantile neuronal ceroid lipofuscinosis (INCL) is a form of neuronal ceroid lipofuscinosis (NCL) characterized by onset during the second half of the first year of life and rapid mental and motor deterioration leading to loss of all psychomotor abilities.

exactMatch

http://identifiers.org/mesh/C537948

http://linkedlifedata.com/resource/umls/id/C0268281

http://linkedlifedata.com/resource/umls/id/C2931673

http://identifiers.org/snomedct/58258004

http://www.orpha.net/ORDO/Orphanet_79263

has exact synonym

Santavuori disease

Santavuori-Haltia disease

INCL

infantile NCL

Hagberg-Santavuori disease

id

MONDO:0019261