Prader-Willi-like syndrome   770680004

SNOMED CT code


SNOMED code770680004
namePrader-Willi-like syndrome
statusactive
date introduced2019-01-31
fully specified name(s)Prader-Willi-like syndrome (disorder)
synonymsPrader-Willi-like syndrome
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteFace structure   89545001
attributes - group3
Pathological processPathological developmental process   308490002
Finding siteGonadal endocrine structure   304041004
OccurrenceCongenital   255399007
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteStructure of distal part of pituitary   52618001
attributes - group4
Has interpretationAbove reference range   281302008
InterpretsBody weight measure   363808001
parents
  • Obesity   414916001
  • Multiple malformation syndrome with unusual brain and/or neuromuscular findings   64162006
  • Multiple malformation syndrome with facial defects as major feature   65094009
  • Congenital hypogonadotropic hypogonadism   722944006
  • Genetic disease   782964007
children
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Obesity   414916001
        Prader-Willi-like syndrome   770680004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Multiple malformation syndrome with unusual brain and/or neuromuscular findings   64162006
                Prader-Willi-like syndrome   770680004

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
              Prader-Willi-like syndrome   770680004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hypogonadotropic hypogonadism   722944006
          Prader-Willi-like syndrome   770680004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Prader-Willi-like syndrome   770680004

ancestors
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