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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:Pseudo-TORCH Syndrome 2
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Accession:DOID:9001536 term browser browse the term
Definition:An autosomal recessive multisystem disorder characterized by antenatal onset of intracranial hemorrhage, calcification, brain malformations, liver dysfunction, and often thrombocytopenia. The disorder results from inappropriate activation of the interferon (IFN) immunologic pathway.
Synonyms:exact_synonym: PTORCH2;   USP18-RELATED CONDITION
 primary_id: MIM:617397



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Pseudo-TORCH Syndrome 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G USP18 ubiquitin specific peptidase 18 ISO ClinVar Annotator: match by term: Pseudo-TORCH syndrome 2 | ClinVar Annotator: match by term: USP18-related condition OMIM
ClinVar
PMID:12833411 PMID:25741868 PMID:27325888 PMID:28492532 PMID:31940699 NCBI chr 5:70,183,321...70,227,990
Ensembl chr 5:70,183,308...70,229,572
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15428
    disease of anatomical entity 15098
      immune system disease 4552
        Pseudo-TORCH Syndrome 2 1
Path 2
Term Annotations click to browse term
  disease 15428
    disease of anatomical entity 15098
      nervous system disease 13250
        central nervous system disease 11838
          brain disease 11112
            disease of mental health 8026
              Neurodevelopmental Disorders 6767
                Developmental Disabilities 758
                  Pseudo-TORCH Syndrome 3
                    Pseudo-TORCH Syndrome 2 1
paths to the root