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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:IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA
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Accession:DOID:9009072 term browser browse the term
Definition:A multisystem disorder characterized by immunodeficiency, mildly delayed psychomotor development, poor overall growth from infancy, and hypohomocysteinemia. (OMIM)
Synonyms:exact_synonym: IMDDHH;   NFE2L2-RELATED CONDITION
 primary_id: MIM:617744
 xref: MONDO:0060591



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IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Nfe2l2 nuclear factor, erythroid derived 2, like 2 ISO ClinVar Annotator: match by term: Immunodeficiency, developmental delay, and hypohomocysteinemia | ClinVar Annotator: match by term: NFE2L2-related condition OMIM
ClinVar
PMID:24130096 PMID:24728327 PMID:25741868 PMID:26619011 PMID:28492532 More... NCBI chr 2:75,505,860...75,535,007
Ensembl chr 2:75,505,857...75,534,985
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16234
    syndrome 10776
      primary immunodeficiency disease 4137
        IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA 1
Path 2
Term Annotations click to browse term
  disease 16234
    disease of anatomical entity 15851
      nervous system disease 13784
        central nervous system disease 12292
          brain disease 11541
            disease of mental health 8326
              Neurodevelopmental Disorders 7016
                Developmental Disabilities 795
                  IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA 1
paths to the root