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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:autosomal dominant microcephaly
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Accession:DOID:14725 term browser browse the term
Definition:A microcephaly that has_material_basis_in heterozygous mutation in an autosomal gene. (DO)
Synonyms:exact_synonym: microcephaly with autosomal dominant inheritance
 primary_id: MESH:C537323
 alt_id: OMIM:156580
For additional species annotation, visit the Alliance of Genome Resources.


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primary autosomal dominant microcephaly 18 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Wdfy3 WD repeat and FYVE domain containing 3 ISO ClinVar Annotator: match by term: Microcephaly 18, primary, autosomal dominant ClinVar
OMIM
PMID:25741868 PMID:27008544 NCBI chr14:7,578,245...7,810,491
Ensembl chr14:7,606,628...7,810,482
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17205
    physical disorder 3086
      congenital nervous system abnormality 1042
        microcephaly 897
          autosomal dominant microcephaly 1
            primary autosomal dominant microcephaly 18 1
Path 2
Term Annotations click to browse term
  disease 17205
    Developmental Disease 10918
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9457
        genetic disease 8960
          monogenic disease 7128
            autosomal genetic disease 6276
              autosomal dominant disease 4460
                complex cortical dysplasia with other brain malformations 1194
                  Malformations of Cortical Development, Group I 1054
                    microcephaly 897
                      autosomal dominant microcephaly 1
                        primary autosomal dominant microcephaly 18 1
paths to the root