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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:neuronal ceroid lipofuscinosis 10
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Accession:DOID:0110725 term browser browse the term
Definition:A neuronal ceroid lipofuscinosis that has_material_basis_in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15. (DO)
Synonyms:exact_synonym: CLN10;   Ceroid Lipofuscinosis, Neuronal, Cathepsin D-Deficient;   cathepsin D deficiency;   congenital neuronal ceroid lipofuscinosis;   neuronal ceroid lipofuscinosis due to cathepsin D deficiency
 narrow_synonym: NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY NEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL
 primary_id: MESH:C566438
 alt_id: OMIA:001505;   OMIM:610127
 xref: GARD:1218;   ORDO:228337


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neuronal ceroid lipofuscinosis 10 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ctsd cathepsin D ISO
ISS		 ClinVar Annotator: match by term: Neuronal ceroid lipofuscinosis 10
CTD Direct Evidence: marker/mechanism
OMIM:610127		 OMIM
ClinVar
CTD
MouseDO		 PMID:10218883 PMID:16670177 PMID:16685649 PMID:24767253 PMID:25298308 More... NCBI chr 1:197,527,467...197,539,343
Ensembl chr 1:197,527,467...197,539,488 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18969
    Nutritional and Metabolic Diseases 8247
      disease of metabolism 8247
        lipid metabolism disorder 1741
          lipid storage disease 832
            neuronal ceroid lipofuscinosis 213
              neuronal ceroid lipofuscinosis 10 1
Path 2
Term Annotations click to browse term
  disease 18969
    Developmental Disease 14400
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13417
        genetic disease 13036
          inherited metabolic disorder 6257
            lipid metabolism disorder 1741
              lipid storage disease 832
                neuronal ceroid lipofuscinosis 213
                  neuronal ceroid lipofuscinosis 10 1
paths to the root