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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:Goldenhar syndrome
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Accession:DOID:2907 term browser browse the term
Definition:A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch. (DO)
Synonyms:exact_synonym: Craniofacial Microsomia;   FAV SEQUENCE;   Facioauriculovertebral Dysplasia;   Facioauriculovertebral Sequence;   Facioauriculovertebral Sequences;   First and Second Branchial Arch Syndrome;   First and Second Pharyngeal Arch Syndromes;   Goldenhar Disease;   Goldenhar Gorlin Syndrome;   Goldenhar Syndrome with Ipsilateral Radial Defect;   Goldenhar-Gorlin Syndromes;   HFM;   Hemifacial Microsomia;   Hemifacial Microsomia with Radial Defects;   Lateral Facial Dysplasia;   Lateral Facial Dysplasias;   Microsomia Hemifacial Radial Defects;   Moeschler Clarren Syndrome;   OAV (oculoauriculovertebral) dysplasia;   OAV DYSPLASIA;   OAVS;   OAVS with Radial Defect;   Oculoauriculovertebral Dysplasia;   Oculoauriculovertebral Dysplasias;   Oculoauriculovertebral Spectrum;   Oculoauriculovertebral Spectrum with Radial Defect;   Oculoauriculovertebral Spectrums;   Oculoauriculovertebral Syndrome;   Oral Mandibular Auricular Syndrome;   Oral-Mandibular-Auricular Syndromes;   craniofacial microsomias;   facio-auriculo-vertebral spectrum;   facioauriculovertebral dysplasias;   first arch syndrome;   otomandibular dysostoses;   otomandibular dysostosis
 primary_id: MESH:D006053
 alt_id: OMIM:141400;   OMIM:164210
 xref: GARD:6540;   NCI:C84740;   ORDO:374
For additional species annotation, visit the Alliance of Genome Resources.



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Goldenhar syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Frk fyn-related Src family tyrosine kinase ISO ClinVar Annotator: match by term: Goldenhar syndrome ClinVar NCBI chr20:38,265,416...38,371,038
Ensembl chr20:38,265,280...38,371,114
JBrowse link
G Pax1 paired box 1 ISO ClinVar Annotator: match by term: Craniofacial microsomia ClinVar NCBI chr 3:134,789,291...134,801,636
Ensembl chr 3:134,789,182...134,801,636
JBrowse link
G Sf3b2 splicing factor 3b, subunit 2 ISO ClinVar Annotator: match by term: Craniofacial microsomia OMIM
ClinVar
PMID:7811205 PMID:34344887 NCBI chr 1:202,570,423...202,590,774
Ensembl chr 1:202,570,423...202,590,759
JBrowse link
G Zic3 Zic family member 3 ISS OMIM:164210 MouseDO NCBI chr  X:136,123,662...136,134,295
Ensembl chr  X:136,124,026...136,134,746
JBrowse link
G Zyg11b zyg-11 family member B, cell cycle regulator ISO ClinVar Annotator: match by term: Goldenhar syndrome ClinVar PMID:25741868 PMID:32738032 NCBI chr 5:122,985,548...123,042,735
Ensembl chr 5:122,992,147...123,042,736
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18215
    syndrome 9746
      Goldenhar syndrome 5
        Axial Mesodermal Dysplasia Spectrum 0
Path 2
Term Annotations click to browse term
  disease 18215
    disease of anatomical entity 17576
      musculoskeletal system disease 7282
        connective tissue disease 5140
          bone disease 3815
            bone development disease 1885
              dysostosis 440
                synostosis 288
                  craniosynostosis 233
                    Crouzon syndrome 29
                      Mandibulofacial Dysostosis 23
                        Goldenhar syndrome 5
                          Axial Mesodermal Dysplasia Spectrum 0
paths to the root