ONTOLOGY REPORT - ANNOTATIONS


Term:Omodysplasia Type 1
go back to main search page
Accession:DOID:9002626 term browser browse the term
Synonyms:exact_synonym: OMOD1;   Omodysplasia autosomal recessive form;   Omodysplasia generalized form;   Omodysplasia, Autosomal Recessive;   omodysplasia (Maroteaux);   omodysplasia 1
 primary_id: MESH:C537746
 alt_id: OMIM:258315;   RDO:0003639
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Omodysplasia Type 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gpc6 glypican 6 JBrowse link 15 102,164,091 103,174,721 RGD:7240710
RGD:8554872
RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    Pathological Conditions, Signs and Symptoms 7745
      Pathologic Processes 4926
        Growth Disorders 244
          Omodysplasia Type 1 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      musculoskeletal system disease 3997
        connective tissue disease 2585
          bone disease 2125
            bone development disease 895
              osteochondrodysplasia 406
                Congenital Micromelic Dysplasia with Dislocation of Radius 1
                  Omodysplasia Type 1 1
paths to the root

NHLBI Logo

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