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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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14314
    syndrome 4612
      Burnett Schwartz Berberian Syndrome 1
        KERATOSIS PILARIS ATROPHICANS 1
Path 2
Term Annotations click to browse term
  disease 14314
    disease of anatomical entity 13524
      nervous system disease 8575
        sensory system disease 4062
          mouth disease 651
            tooth disease 222
              Tooth Abnormalities 104
                dental enamel hypoplasia 32
                  amelogenesis imperfecta 30
                    X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 1
                      Burnett Schwartz Berberian Syndrome 1
                        KERATOSIS PILARIS ATROPHICANS 1
paths to the root