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Methionine Malabsorption Syndrome - Ontology Report - Rat Genome Database

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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:Methionine Malabsorption Syndrome
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Accession:DOID:9006082 term browser browse the term
Synonyms:exact_synonym: Oasthouse Urine Disease;   Smith-Strang Disease
 primary_id: MESH:C562682
 alt_id: MIM:250900


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Path 1
Term Annotations click to browse term
  disease 19106
    syndrome 11278
      Methionine Malabsorption Syndrome 0
Path 2
Term Annotations click to browse term
  disease 19106
    disease of anatomical entity 18445
      nervous system disease 14349
        Neurologic Manifestations 10433
          sensory system disease 7336
            eye disease 3682
              visual pathway disease 198
                visual cortex disease 195
                  visual epilepsy 195
                    Methionine Malabsorption Syndrome 0
paths to the root