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ONTOLOGY REPORT - ANNOTATIONS


Term:Burnett Schwartz Berberian Syndrome
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Accession:DOID:9000847 term browser browse the term
Synonyms:exact_synonym: Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2;   Atrophodermia Reticulata Symmetrica Faciei;   Atrophodermia reticulata;   Atrophodermia vermiculata;   Folliculitis ulerythematosa;   Folliculitis ulerythematosa reticulata;   Honeycomb atrophy;   Keratosis Pilaris Atrophicans Facies;   Keratosis pilaris;   Ulerythema ophryogenes;   Ulerythema ophryogenes with multiple congenital anomalies;   Ulerythema ophryogenesis
 primary_id: MESH:C537412;   RDO:0003253
For additional species annotation, visit the Alliance of Genome Resources.


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Burnett Schwartz Berberian Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lrp1 LDL receptor related protein 1 JBrowse link 7 70,846,313 70,927,028 RGD:8554872
KERATOSIS PILARIS ATROPHICANS term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lrp1 LDL receptor related protein 1 JBrowse link 7 70,846,313 70,927,028 RGD:11554173
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    syndrome 4210
      Burnett Schwartz Berberian Syndrome 1
        KERATOSIS PILARIS ATROPHICANS 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        sensory system disease 4231
          mouth disease 655
            tooth disease 221
              Tooth Abnormalities 100
                dental enamel hypoplasia 30
                  amelogenesis imperfecta 28
                    X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 1
                      Burnett Schwartz Berberian Syndrome 1
                        KERATOSIS PILARIS ATROPHICANS 1
paths to the root