Term:Facial Ectodermal Dysplasia
go back to main search page
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.

show annotations for term's descendants       view all columns           Sort by:
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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    sensory system disease 4246
      skin disease 2253
        Facial Ectodermal Dysplasia 1
Path 2
Term Annotations click to browse term
  disease 14875
    Developmental Diseases 7711
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6750
        genetic disease 5997
          monogenic disease 2855
            X-linked monogenic disease 490
              X-linked dominant disease 61
                focal dermal hypoplasia 3
                  Facial Ectodermal Dysplasia 1
paths to the root


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