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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:Polymicrogyria with or without Vascular-Type Ehlers-Danlos Syndrome
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Accession:DOID:9000950 term browser browse the term
Definition:An autosomal recessive disorder with a highly variable phenotype. Although all patients have polymicrogyria and other variable structural brain anomalies on imaging, only some show developmental delay and/or seizures.
Synonyms:exact_synonym: PMGEDSV;   Polymicrogyria with or without vascular-type EDS
 narrow_synonym: POLYMICROGYRIA WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME
 primary_id: OMIM:618343
For additional species annotation, visit the Alliance of Genome Resources.


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Polymicrogyria with or without Vascular-Type Ehlers-Danlos Syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Col3a1 collagen type III alpha 1 chain ISO OMIM NCBI chrNW_004955403:9,720,831...9,758,019
Ensembl chrNW_004955403:9,721,114...9,757,887
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12519
    syndrome 6288
      Ehlers-Danlos syndrome 102
        Ehlers-Danlos Syndrome Type 4 4
          vascular type Ehlers-Danlos syndrome 1
            Polymicrogyria with or without Vascular-Type Ehlers-Danlos Syndrome 1
Path 2
Term Annotations click to browse term
  disease 12519
    Developmental Disease 9309
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7860
        genetic disease 7447
          monogenic disease 5732
            autosomal genetic disease 5026
              autosomal dominant disease 3403
                complex cortical dysplasia with other brain malformations 1118
                  Malformations of Cortical Development, Group III 19
                    Polymicrogyria 13
                      Polymicrogyria with or without Vascular-Type Ehlers-Danlos Syndrome 1
paths to the root