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RGD uses the Human Disease Ontology (DO, 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:X-linked panhypopituitarism
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Accession:DOID:0111779 term browser browse the term
Definition:A panhypopituitarism that has_material_basis_in duplications in SOX3 on chromosome Xq27.1. (DO)
Synonyms:exact_synonym: PHPX;   pituitary dwarfism IV
 primary_id: MESH:C538613
 alt_id: OMIM:312000
 xref: GARD:6737
For additional species annotation, visit the Alliance of Genome Resources.

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X-linked panhypopituitarism term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Sox3 SRY-box transcription factor 3 ISO ClinVar Annotator: match by OMIM:312000 OMIM
PMID:15800844 NCBI chr  X:139,308,608...139,310,734
Ensembl chr  X:139,309,329...139,310,678
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17289
    Developmental Disease 10990
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9530
        genetic disease 9033
          monogenic disease 7190
            X-linked monogenic disease 1027
              X-linked panhypopituitarism 1
Path 2
Term Annotations click to browse term
  disease 17289
    disease of anatomical entity 16625
      nervous system disease 12154
        central nervous system disease 10420
          brain disease 9782
            thalamic disease 227
              hypothalamic disease 227
                pituitary gland disease 172
                  hypopituitarism 46
                    panhypopituitarism 10
                      X-linked panhypopituitarism 1
paths to the root