ONTOLOGY REPORT - ANNOTATIONS


Term:Focal Facial Dermal Dysplasia
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Accession:DOID:9005418 term browser browse the term
Synonyms:exact_synonym: Bitemporal aplasia cutis congenita;   Brauer syndrome;   FFDD, type 1;   FFDD1;   Hereditary symmetrical aplastic nevi of temples
 primary_id: MESH:C537068
 alt_id: OMIM:136500;   RDO:0002835
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Focal Facial Dermal Dysplasia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cyp26c1 cytochrome P450, family 26, subfamily C, polypeptide 1 JBrowse link 1 256,369,410 256,380,649 RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    syndrome 4218
      ectodermal dysplasia 142
        focal dermal hypoplasia 3
          Focal Facial Dermal Dysplasia 1
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        sensory system disease 4244
          skin disease 2253
            Skin Abnormalities 344
              ectodermal dysplasia 142
                focal dermal hypoplasia 3
                  Focal Facial Dermal Dysplasia 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.