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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:Primary Autosomal Recessive Microcephaly 26
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Accession:DOID:9006542 term browser browse the term
Definition:Characterized by progressive microcephaly beginning at birth and associated with global developmental delay with variably impaired intellectual development. Caused by heterozygous mutation in the LMNB1 gene on chromosome 5q23.
Synonyms:exact_synonym: MCPH26
 broad_synonym: LMNB1-RELATED CONDITION
 related_synonym: MICROCEPHALY 26, PRIMARY, AUTOSOMAL DOMINANT
 primary_id: OMIM:619179



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Primary Autosomal Recessive Microcephaly 26 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Lmnb1 lamin B1 ISO ClinVar Annotator: match by term: LMNB1-related condition | ClinVar Annotator: match by term: Microcephaly 26, primary, autosomal dominant OMIM
ClinVar
PMID:25741868 PMID:32910914 PMID:33033404 NCBI chr18:50,175,861...50,215,210
Ensembl chr18:50,175,874...50,214,502
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21155
    physical disorder 4941
      congenital nervous system abnormality 1482
        microcephaly 1122
          primary microcephaly 44
            primary autosomal recessive microcephaly 34
              Primary Autosomal Recessive Microcephaly 26 1
Path 2
Term Annotations click to browse term
  disease 21155
    Developmental Disease 18469
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18327
        genetic disease 18271
          monogenic disease 10324
            autosomal genetic disease 9470
              autosomal dominant disease 6224
                complex cortical dysplasia with other brain malformations 1583
                  Malformations of Cortical Development, Group I 1371
                    microcephaly 1122
                      primary microcephaly 44
                        primary autosomal recessive microcephaly 34
                          Primary Autosomal Recessive Microcephaly 26 1
paths to the root