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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:Manz Syndrome
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Accession:DOID:9008129 term browser browse the term
Synonyms:exact_synonym: Familial hypomagnesemia - hypercalciuria
 primary_id: MESH:C535709
 alt_id: RDO:0000975
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 18156
    syndrome 9705
      Manz Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18156
    Nutritional and Metabolic Diseases 6770
      disease of metabolism 6770
        acquired metabolic disease 2157
          nutrition disease 1045
            Malnutrition 313
              nutritional deficiency disease 302
                primary hypomagnesemia 7
                  Manz Syndrome 0
paths to the root