Pierre Robin sequence faciodigital anomaly syndrome   723461007

SNOMED CT code


SNOMED code723461007
namePierre Robin sequence faciodigital anomaly syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Pierre Robin sequence faciodigital anomaly syndrome (disorder)
synonyms
  • Pierre Robin sequence faciodigital anomaly syndrome
  • Chitayat Meunier Hodgkinson syndrome
  • Pierre Robin sequence with facial and digital anomalies
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteFace structure   89545001
OccurrenceCongenital   255399007
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteDigit structure   82680008
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              X-linked recessive hereditary disease   1162976004
                Pierre Robin sequence faciodigital anomaly syndrome   723461007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Pierre Robin sequence faciodigital anomaly syndrome   723461007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Disorder of digit   128597007
          Congenital anomaly of digit   403855001
            Pierre Robin sequence faciodigital anomaly syndrome   723461007

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
              Robin sequence   4602007
                Pierre Robin sequence faciodigital anomaly syndrome   723461007

ancestors
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