Mutilating keratoderma   24559001

SNOMED CT code


SNOMED code24559001
nameMutilating keratoderma
statusactive
date introduced2002-01-31
fully specified name(s)Mutilating keratoderma (disorder)
synonyms
  • Vohwinkel's mutilating keratoderma
  • Mutilating keratoderma
  • Keratoderma hereditarium mutilans
  • Mutilating keratoderma of Vohwinkel
  • Vohwinkel syndrome
attributes - group3
Associated morphologyHyperkeratosis   26996000
Finding siteSkin structure of sole of foot   37136002
attributes - group2
Finding siteSkin structure of palmar area of hand   70887009
Associated morphologyHyperkeratosis   26996000
attributes - group4
InterpretsHearing   47078008
Has interpretationImpaired   260379002
attributes - group5
OccurrenceCongenital   255399007
Finding siteAuditory structure   91159003
attributes - group1
Has interpretationAbnormal   263654008
InterpretsKeratinization   44138005
parents
children
  • Autosomal dominant mutilating keratoderma   239068002  removed: 2021-09-30
  • Keratoderma hereditarium mutilans with ichthyosis syndrome   717183001
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
              Mutilating keratoderma   24559001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Hereditary palmoplantar keratoderma   239066003
            Mutilating keratoderma   24559001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Disorder of keratinization   277905003
          Inherited disorder of keratinization   254214009
            Erythrokeratoderma   254215005
              Mutilating keratoderma   24559001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Ear and auditory finding   118236001
      Disorder of auditory system   362966006
        Auditory system hereditary disorder   362991006
          Mutilating keratoderma   24559001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hearing disorder   95827002
          Congenital sensorineural hearing loss   700453005
            Mutilating keratoderma   24559001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Finding of upper limb   116307009
        Finding of hand region   116311003
          Rough skin of hands   829993001
            Mutilating keratoderma   24559001

ancestors
sorted most to least specific
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