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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:syndromic microphthalmia 12
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Accession:DOID:0111800 term browser browse the term
Definition:A syndromic microphthalmia characterized by bilateral microphthalmia, pulmonary hypoplasia, and diaphragmatic hernia that has_material_basis_in compound heterozygous or heterozygous mutation in RARB on chromosome 3p24.2. (DO)
Synonyms:exact_synonym: MCOPS12;   Microphthalmia with or without Pulmonary Hypoplasia, Diaphragmatic Hernia, and/or Cardiac Defects
 primary_id: OMIM:615524
 xref: GARD:13235
For additional species annotation, visit the Alliance of Genome Resources.


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syndromic microphthalmia 12 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G RARB retinoic acid receptor beta ISO OMIM NCBI chr 3:24,729,220...25,499,187
Ensembl chr 3:25,660,922...25,833,297
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12807
    sensory system disease 4762
      eye disease 2437
        microphthalmia 89
          syndromic microphthalmia 20
            syndromic microphthalmia 12 1
Path 2
Term Annotations click to browse term
  disease 12807
    disease of anatomical entity 12337
      nervous system disease 10078
        sensory system disease 4762
          eye disease 2437
            Eye Abnormalities 343
              microphthalmia 89
                syndromic microphthalmia 20
                  syndromic microphthalmia 12 1
paths to the root