Syndromic orbital border hypoplasia   717337001

SNOMED CT code


SNOMED code717337001
nameSyndromic orbital border hypoplasia
statusactive
date introduced2016-07-31
fully specified name(s)Syndromic hypoplasia of orbital border (disorder)
synonyms
  • Syndromic orbital border hypoplasia
  • Urrets Zavalia syndrome
  • Syndromic hypoplasia of orbital border
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyHypoplasia   55199003
Finding siteOrbital margin structure   77886003
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteFace structure   89545001
parents
  • Autosomal dominant hereditary disorder   11164009
  • Orbital margin finding   246913001
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of the visual system   363343008
  • Congenital anomaly of orbit   54873004
  • Multiple malformation syndrome with facial defects as major feature   65094009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Syndromic orbital border hypoplasia   717337001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Orbit finding   246912006
        Orbital margin finding   246913001
          Syndromic orbital border hypoplasia   717337001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Syndromic orbital border hypoplasia   717337001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Syndromic orbital border hypoplasia   717337001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Congenital anomaly of visual system   127329003
          Congenital anomaly of orbit   54873004
            Syndromic orbital border hypoplasia   717337001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of face   118930001
          Congenital anomaly of face   398302004
            Multiple malformation syndrome with facial defects as major feature   65094009
              Syndromic orbital border hypoplasia   717337001

ancestors
sorted most to least specific
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