Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   


RGD uses the Human Disease Ontology (DO, 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
go back to main search page
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. (OMIM)
Synonyms:exact_synonym: PTORCH2
 primary_id: OMIM:617397
 alt_id: RDO:9001724
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12748
    disease of anatomical entity 12278
      immune system disease 2465
        Pseudo-TORCH Syndrome 2 0
Path 2
Term Annotations click to browse term
  disease 12748
    disease of anatomical entity 12278
      nervous system disease 10025
        central nervous system disease 8471
          brain disease 7847
            disease of mental health 5733
              Neurodevelopmental Disorders 4530
                Developmental Disabilities 639
                  Pseudo-TORCH Syndrome 2
                    Pseudo-TORCH Syndrome 2 0
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.