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Term:Larsen syndrome
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Accession:DOID:14764 term browser browse the term
Definition:An autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities. (DO)
Synonyms:exact_synonym: LRS;   Larsen Syndrome, Autosomal Dominant;   Larsen syndrome, dominant type;   dominant Larsen syndrome
 related_synonym: FLNB-related spectrum disorder;   FLNB-related spectrum disorders
 primary_id: MESH:C537873
 alt_id: OMIM:150250;   RDO:0003785
 xref: GARD:6860
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Larsen syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Chst3 carbohydrate sulfotransferase 3 JBrowse link 10 60,181,527 60,222,114 RGD:8554872
G Flnb filamin, beta JBrowse link 14 7,817,921 7,951,588 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12521
    Wounds and Injuries 803
      Joint Dislocations 12
        Larsen syndrome 2
Path 2
Term Annotations click to browse term
  disease 12521
    Developmental Diseases 8507
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7274
        Congenital Abnormalities 3566
          Musculoskeletal Abnormalities 1305
            Craniofacial Abnormalities 1056
              Maxillofacial Abnormalities 205
                Jaw Abnormalities 203
                  orofacial cleft 114
                    cleft palate 92
                      Larsen syndrome 2
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.