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RGD uses the Human Disease Ontology (DO, 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:Meckel Syndrome, Type 10
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Accession:DOID:9004364 term browser browse the term
Synonyms:exact_synonym: MKS10
 narrow_synonym: JBTS34;   Joubert syndrome 34
 primary_id: OMIM:614175
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12699
    syndrome 6161
      ciliopathy 224
        Meckel syndrome 28
          Meckel Syndrome, Type 10 0
Path 2
Term Annotations click to browse term
  disease 12699
    Developmental Diseases 8992
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7841
        genetic disease 7381
          monogenic disease 5444
            ciliopathy 224
              Joubert syndrome 76
                Meckel Syndrome, Type 10 0
paths to the root


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