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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:Hallermann-Streiff syndrome
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Accession:DOID:4534 term browser browse the term
Definition:A syndrome that affects growth, cranial development, hair growth and dental development. (DO)
Synonyms:exact_synonym: Francois Dyscephalic Syndrome;   Francois dyscephalic syndromes;   HSS;   Hallerman-Streiff syndrome;   Hallermann syndrome;   Hallermann's syndrome;   Hallermann-Streiff-Francois syndrome;   Hallermanns Syndrome
 primary_id: MESH:D006210
 alt_id: OMIM:234100
 xref: GARD:288;   NCI:C84746;   ORDO:2108
For additional species annotation, visit the Alliance of Genome Resources.



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17773
    syndrome 10064
      Hallermann-Streiff syndrome 0
        Dennis Fairhurst Moore Syndrome 0
Path 2
Term Annotations click to browse term
  disease 17773
    disease of anatomical entity 15145
      musculoskeletal system disease 7742
        connective tissue disease 5279
          bone disease 3826
            bone development disease 2275
              dysostosis 575
                synostosis 371
                  craniosynostosis 312
                    Crouzon syndrome 30
                      Hallermann-Streiff syndrome 0
                        Dennis Fairhurst Moore Syndrome 0
paths to the root