Send us a Message



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

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:immunodeficiency 31C
go back to main search page
Accession:DOID:0111946 term browser browse the term
Definition:A primary immunodeficiency disease characterized by onset in infancy or childhood of chronic mucocutaneous candidiasis and increased IFNG activation that has_material_basis_in heterozygous gain of function mutation in the STAT1 gene on chromosome 2q32.2. (DO)
Synonyms:exact_synonym: CANDF7;   IMD31C;   autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome;   autosomal dominant immunodeficiency 31C;   familial candidiasis 7
 broad_synonym: familial chronic mucocutaneous candidiasis, autosomal dominant
 primary_id: OMIM:614162
 xref: NCI:C172099;   ORDO:391487


GViewer not supported for the selected species.

show annotations for term's descendants           Sort by:
immunodeficiency 31C term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Il21r interleukin 21 receptor ISO ClinVar Annotator: match by term: Immunodeficiency 31C ClinVar PMID:25741868 NCBI chrNW_004624782:12,037,338...12,070,479
Ensembl chrNW_004624782:12,057,651...12,068,650
JBrowse link
G Stat1 signal transducer and activator of transcription 1 ISO ClinVar Annotator: match by term: Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome | ClinVar Annotator: match by term: Candidiasis, familial, 7 | ClinVar Annotator: match by term: Immunodeficiency 31C OMIM
ClinVar
PMID:9536098 PMID:17576681 PMID:21714643 PMID:21727188 PMID:22195034 More... NCBI chrNW_004624854:5,067,578...5,106,052
Ensembl chrNW_004624854:5,067,535...5,102,106
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14088
    syndrome 9293
      primary immunodeficiency disease 3444
        immunodeficiency 31C 2
Path 2
Term Annotations click to browse term
  disease 14088
    Pathological Conditions, Signs and Symptoms 10990
      Signs and Symptoms 9102
        Neurologic Manifestations 8807
          sensory system disease 6153
            skin disease 3489
              Infectious Skin Diseases 225
                dermatomycosis 86
                  chronic mucocutaneous candidiasis 52
                    immunodeficiency 31C 2
paths to the root