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ONTOLOGY REPORT - ANNOTATIONS


Term:Hypomyelinating Leukodystrophy 19
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Accession:DOID:9006466 term browser browse the term
Synonyms:exact_synonym: HLD19;   hypomyelinating leukodystrophy 19, transient infantile
 primary_id: OMIM:618688
For additional species annotation, visit the Alliance of Genome Resources.


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Hypomyelinating Leukodystrophy 19 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tmem63a transmembrane protein 63a JBrowse link 13 99,219,585 99,253,176 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15502
    Developmental Diseases 8872
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7669
        genetic disease 7157
          Nervous System Heredodegenerative Disorders 1728
            Hereditary Central Nervous System Demyelinating Diseases 39
              hypomyelinating leukodystrophy 23
                Hypomyelinating Leukodystrophy 19 1
Path 2
Term Annotations click to browse term
  disease 15502
    disease of anatomical entity 14856
      nervous system disease 10270
        central nervous system disease 8409
          brain disease 7762
            Metabolic Brain Diseases 481
              Metabolic Brain Diseases, Inborn 414
                Hereditary Central Nervous System Demyelinating Diseases 39
                  hypomyelinating leukodystrophy 23
                    Hypomyelinating Leukodystrophy 19 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.