SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Hecht syndrome   8757006

SNOMED CT code


SNOMED code8757006
nameHecht syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Hecht syndrome (disorder)
synonyms
  • Hecht syndrome
  • Trismus pseudocamptodactyly syndrome
  • Distal arthrogryposis type 7
  • Dutch Kentucky syndrome
  • Hecht Beals syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Finding siteStructure of joint region   785818007
Associated morphologyContracture   57048009
OccurrenceCongenital   255399007
attributes - group2
InterpretsRange of joint movement   364564000
Has interpretationDecreased   1250004
parents
  • Autosomal dominant hereditary disorder   11164009
  • Distal arthrogryposis syndrome   24269006
  • Inherited arthrogryposis   28204005
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
              Hecht syndrome   8757006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Deformity   417893002
      Congenital deformity   276655000
        Arthrogryposis   111246005
          Distal arthrogryposis syndrome   24269006
            Hecht syndrome   8757006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Inherited arthrogryposis   28204005
            Hecht syndrome   8757006

ancestors
sorted most to least specific
cpt crosswalks

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