SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Angelman syndrome  76880004

Angelman syndrome due to maternal monosomy 15q11q13   1162462009

SNOMED CT code


SNOMED code1162462009
nameAngelman syndrome due to maternal monosomy 15q11q13
statusactive
date introduced2021-09-30
fully specified name(s)Angelman syndrome due to maternal monosomy 15q11q13 (disorder)
synonymsAngelman syndrome due to maternal monosomy 15q11q13
attributes - group1
OccurrenceCongenital   255399007
Finding siteNervous system structure   25087005
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
attributes - group2
OccurrenceCongenital   255399007
Finding siteFace structure   89545001
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
attributes - group3
InterpretsIntellectual ability   247573007
Has interpretationImpaired   260379002
attributes - group4
InterpretsAdaptation behavior   406208005
Has interpretationImpaired   260379002
parentsAngelman syndrome   76880004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Angelman syndrome   76880004
          Angelman syndrome due to maternal monosomy 15q11q13   1162462009

ancestors
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