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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:Nestor-Guillermo progeria syndrome
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Accession:DOID:0081334 term browser browse the term
Definition:A progeroid syndrome that is characterized by lipoatrophy, osteoporosis, and very severe osteolysis. Patients have no cardiovascular impairment, diabetes mellitus, or hypertriglyceridemia, but suffer profound skeletal abnormalities that affect their quality of life and that has_material_basis_in homozygous mutation in the BANF1 gene on chromosome 11q13. Onset is after 2 years of age. (DO)
Synonyms:exact_synonym: NGPS;   PROGERIA SYNDROME, CHILDHOOD-ONSET, WITH OSTEOLYSIS;   PSCOO
 primary_id: MIM:614008
 alt_id: DOID:9000907
 xref: GARD:11008;   ORDO:280576


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Nestor-Guillermo progeria syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Banf1 BAF nuclear assembly factor 1 ISO ClinVar Annotator: match by term: Nestor-Guillermo progeria syndrome OMIM
ClinVar		 PMID:21549337 PMID:23720404 PMID:28492532 NCBI chr19:5,414,661...5,416,904
Ensembl chr19:5,414,666...5,417,196 		JBrowse link
G Eif1ad eukaryotic translation initiation factor 1A domain containing ISO ClinVar Annotator: match by term: Nestor-Guillermo progeria syndrome ClinVar NCBI chr19:5,416,841...5,421,546
Ensembl chr19:5,416,769...5,421,554 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16177
    syndrome 10682
      progeroid syndrome 27
        Nestor-Guillermo progeria syndrome 2
Path 2
Term Annotations click to browse term
  disease 16177
    Developmental Disease 13928
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 12950
        genetic disease 12639
          monogenic disease 10691
            autosomal genetic disease 9881
              autosomal dominant disease 6550
                progeria 20
                  Progeria Syndrome, Childhood-Onset 3
                    Nestor-Guillermo progeria syndrome 2
paths to the root