FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term neuronal ceroid lipofuscinosis ID (Ontology) DOID:14503 (Human Disease)
Definition
Also Known As "hereditary ceroid lipofuscinosis"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      11
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 neuronal ceroid lipofuscinosis      11      9      1
 exacerbates | neuronal ceroid lipofuscinosis       7       --       --
 model of | neuronal ceroid lipofuscinosis       4       --       --
Spanning Tree (Parents/Children)
Only view relationship: 
  lysosomal storage disease
   |__lipid storage disease
       |__neuronal ceroid lipofuscinosis  62 rec.
           |__neuronal ceroid lipofuscinosis 1 9 rec.
           |__neuronal ceroid lipofuscinosis 2
           |__neuronal ceroid lipofuscinosis 3 2 rec.
           |__neuronal ceroid lipofuscinosis 4 17 rec.
           |__neuronal ceroid lipofuscinosis 5
           |__neuronal ceroid lipofuscinosis 6A
           |__neuronal ceroid lipofuscinosis 6B
           |__neuronal ceroid lipofuscinosis 7 9 rec.
           |__neuronal ceroid lipofuscinosis 8 1 rec.
           |__neuronal ceroid lipofuscinosis 8 northern epilepsy variant 1 rec.
           |__neuronal ceroid lipofuscinosis 9
           |__neuronal ceroid lipofuscinosis 10 3 rec.
           |__neuronal ceroid lipofuscinosis 11
           |__neuronal ceroid lipofuscinosis 13 2 rec.
           |__neuronal ceroid lipofuscinosis 15 1 rec.
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Is a lipid storage disease
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Synonyms
  • "hereditary ceroid lipofuscinosis" EXACT
Secondary IDs
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GARD:10739
ICD10CM:E75.4
MESH:D009472
MIM:PS256730
NCI:C61257
ORDO:216
ORDO:79262
SNOMEDCT_US_2023_03_01:42012007
UMLS_CUI:C0027877