Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP 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:rhizomelic chondrodysplasia punctata type 2
go back to main search page
Accession:DOID:0110852 term browser browse the term
Definition:A rhizomelic chondrodysplasia punctata that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the GNPAT gene on chromosome 1q42.2. (DO)
Synonyms:exact_synonym: Chondrodysplasia Punctata, Rhizomelic, Due To Dihydroxyacetonephosphate Acyltransferase Deficiency;   Chondrodysplasia punctata, rhizomelic, due to DHAPAT deficiency;   DHAPAT deficiency;   Dihydroxyacetonephosphate acyltransferase deficiency;   GNPAT deficiency;   Glyceronephosphate O-Acyltransferase Deficiency;   Glyceronephosphate acyltransferase deficiency;   Human dihydroxyacetonephosphate acyltransferase deficiency;   Peroxisomal dihydroxyacetonephosphate acyltransferase deficiency;   RCDP2
 primary_id: MESH:C537607;   RDO:0003477
 alt_id: OMIM:222765
 xref: ORDO:309796
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
rhizomelic chondrodysplasia punctata type 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gnpat glyceronephosphate O-acyltransferase ISO ClinVar Annotator: match by OMIM:222765
ClinVar Annotator: match by term: Rhizomelic chondrodysplasia punctata type 2
OMIM
ClinVar
PMID:1405476 PMID:7530787 PMID:9536089 PMID:9843043 PMID:11152660 PMID:21990100 PMID:24033266 PMID:25741868 PMID:28492532 NCBI chr19:57,614,813...57,640,524
Ensembl chr19:57,614,628...57,640,726
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16092
    syndrome 7036
      chondrodysplasia punctata 7
        rhizomelic chondrodysplasia punctata 4
          rhizomelic chondrodysplasia punctata type 2 1
Path 2
Term Annotations click to browse term
  disease 16092
    disease of anatomical entity 15341
      musculoskeletal system disease 5736
        connective tissue disease 4135
          bone disease 3505
            bone development disease 1305
              osteochondrodysplasia 442
                chondrodysplasia punctata 7
                  rhizomelic chondrodysplasia punctata 4
                    rhizomelic chondrodysplasia punctata type 2 1
paths to the root