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ONTOLOGY REPORT - ANNOTATIONS


Term:MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY
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Accession:DOID:9007395 term browser browse the term
Synonyms:exact_synonym: MCT1D
 narrow_synonym: MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL DOMINANT;   MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL RECESSIVE
 primary_id: OMIM:616095;   RDO:9001197
For additional species annotation, visit the Alliance of Genome Resources.


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MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc16a1 solute carrier family 16 member 1 JBrowse link 2 207,108,552 207,129,352 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY 1
Path 2
Term Annotations click to browse term
  disease 14924
    Nutritional and Metabolic Diseases 4249
      disease of metabolism 4249
        Acid-Base Imbalance 72
          Acidoses 60
            Ketosis 7
              MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.