FTP Download
Chinchilla Research Resource Database
   
Keyword
  

ONTOLOGY REPORT - ANNOTATIONS


Term:Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2
go back to main search page
Accession:DOID:9005669 term browser browse the term
Synonyms:exact_synonym: MDDGB2;   MUSCULAR DYSTROPHY, CONGENITAL, POMT2-RELATED
 primary_id: OMIM:613156
 alt_id: RDO:0009889
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pomt2 protein-O-mannosyltransferase 2 JBrowse link 6 111,137,329 111,176,991 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    Developmental Diseases 7628
      Neurodevelopmental Disorders 2745
        intellectual disability 1146
          Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        peripheral nervous system disease 1998
          neuropathy 1823
            neuromuscular disease 1406
              muscular disease 902
                muscle tissue disease 631
                  atrophic muscular disease 243
                    muscular dystrophy 242
                      congenital muscular dystrophy 60
                        muscular dystrophy-dystroglycanopathy 16
                          Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 1
paths to the root