Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT code


SNOMED code1172635005
nameSplit-foot malformation, mesoaxial polydactyly syndrome
statusactive
date introduced2021-09-30
fully specified name(s)Split-foot malformation, mesoaxial polydactyly syndrome (disorder)
synonyms
  • SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome
  • Split-foot malformation, mesoaxial polydactyly syndrome
  • Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome
attributes - group5
InterpretsHearing   47078008
Has interpretationImpaired   260379002
attributes - group1
OccurrenceCongenital   255399007
Finding siteFoot structure   56459004
Associated morphologyDevelopmental failure of fusion   371520008
Pathological processPathological developmental process   308490002
attributes - group2
OccurrenceCongenital   255399007
Finding siteEntire lesser toe   182308006
Associated morphologyAbsence   418560003
Pathological processPathological developmental process   308490002
attributes - group3
OccurrenceCongenital   255399007
Finding siteStructure of nail unit of digit of hand   770804008
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
attributes - group4
OccurrenceCongenital   255399007
Finding siteAuditory structure   91159003
attributes - group6
Finding siteLeft ear structure   89644007
attributes - group7
Finding siteRight ear structure   25577004
parents
  • Sensorineural hearing loss of bilateral ears   194424005
  • Split foot   205358006
  • Hearing loss associated with syndrome   232333009
  • Finding of digit of hand   313132009
  • Congenital anomaly of hand   34111000
  • Congenital anomaly of nail   35964007
  • Auditory system hereditary disorder   362991006
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of the integument   363185004
  • Disorder of skin of upper limb   400160003
  • Genetic disorder of nail   402775007
  • Multiple malformation syndrome with limb defect as major feature   41443008
  • Congenital sensorineural hearing loss   700453005
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Hearing finding   118230007
        Hearing disorder   128540005
          Hearing loss   15188001
            Hearing loss in left ear   1088891000119106
              Sensorineural hearing loss of bilateral ears   194424005
                Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Finding of lower limb   116312005
        Absence of lower limb   723722000
          Congenital absence of foot   371197005
            Congenital absence of toe   66345008
              Split foot   205358006
                Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Hearing finding   118230007
        Hearing disorder   128540005
          Hearing loss   15188001
            Hearing loss associated with syndrome   232333009
              Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Finding of upper limb   116307009
        Finding of hand region   116311003
          Finding of digit of hand   313132009
            Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Finding of upper limb   116307009
        Finding of hand region   116311003
          Disorder of hand   118933004
            Congenital anomaly of hand   34111000
              Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental abnormality of nail   238715009
          Congenital anomaly of nail   35964007
            Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Ear and auditory finding   118236001
      Disorder of auditory system   362966006
        Auditory system hereditary disorder   362991006
          Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Skin finding   106076001
        Disorder of skin   95320005
          Disorder of skin of upper limb   400160003
            Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic disorder of nail   402775007
          Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

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 limb defect as major feature   41443008
                Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hearing disorder   95827002
          Congenital sensorineural hearing loss   700453005
            Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Split-foot malformation, mesoaxial polydactyly syndrome   1172635005

ancestors
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