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ONTOLOGY REPORT - ANNOTATIONS


Term:Facial Ectodermal Dysplasia
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Accession:DOID:9003398 term browser browse the term
Synonyms:exact_synonym: Bitemporal forceps marks syndrome;   FFDD3;   Focal Facial Dermal Dysplasia 3, Setleis Type;   Focal Facial Dermal Dysplasia, Type II;   Focal facial dermal dysplasia type 2;   Setleis syndrome
 primary_id: MESH:C536385;   RDO:0001951
 alt_id: OMIM:227260
For additional species annotation, visit the Alliance of Genome Resources.


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Facial Ectodermal Dysplasia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Twist2 twist family bHLH transcription factor 2 JBrowse link 9 98,924,134 98,968,510 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    sensory system disease 4231
      skin disease 2240
        Facial Ectodermal Dysplasia 1
Path 2
Term Annotations click to browse term
  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          monogenic disease 2854
            X-linked monogenic disease 490
              X-linked dominant disease 54
                focal dermal hypoplasia 3
                  Facial Ectodermal Dysplasia 1
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