Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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:MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS
go back to main search page
Accession:DOID:9002853 term browser browse the term
Definition:An inborn error of cholesterol metabolism that is characterized by accumulation of a large amount of methylsterols, particularly dimethylsterols. (OMIM)
Synonyms:exact_synonym: MCCPD;   MICROCEPHALY, CONGENITAL CATARACTS, AND PSORIASIFORM DERMATITIS;   SC4MOL DEFICIENCY
 primary_id: OMIM:616834;   RDO:9000354
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G MSMO1 methylsterol monooxygenase 1 ISO OMIM NCBI chr 4:157,523,099...157,538,508
Ensembl chr 4:169,606,809...169,622,212
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13787
    physical disorder 2970
      congenital nervous system abnormality 1015
        microcephaly 890
          MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS 1
Path 2
Term Annotations click to browse term
  disease 13787
    Developmental Disease 10362
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8916
        genetic disease 8458
          monogenic disease 6878
            autosomal genetic disease 6075
              autosomal dominant disease 4336
                complex cortical dysplasia with other brain malformations 1181
                  Malformations of Cortical Development, Group I 1046
                    microcephaly 890
                      MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS 1
paths to the root