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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:Peptide Growth Factors Deficiency
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Accession:DOID:9003140 term browser browse the term
Synonyms:exact_synonym: Hoepffner dreyer reimers syndrome;   Peptidic growth factors deficiency
 primary_id: MESH:C536656;   RDO:0002297


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    Diseases of the Aged 1467
      Premature Aging 72
        Werner syndrome 5
          Peptide Growth Factors Deficiency 0
Path 2
Term Annotations click to browse term
  disease 21128
    Developmental Disease 18449
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18309
        genetic disease 18253
          monogenic disease 10363
            autosomal genetic disease 9517
              autosomal recessive disease 6583
                Werner syndrome 5
                  Peptide Growth Factors Deficiency 0
paths to the root