SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Autosomal dominant variant form of albumin   21367009

SNOMED CT code


SNOMED code21367009
nameAutosomal dominant variant form of albumin
statusactive
date introduced2002-01-31
fully specified name(s)Autosomal dominant variant form of albumin (disorder)
synonymsAutosomal dominant variant form of albumin
attributes - group1
OccurrenceCongenital   255399007
Finding siteThyroid structure   69748006
parents
  • Autosomal dominant hereditary disorder   11164009
  • Thyroxine transport defect   56112001
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
              Autosomal dominant variant form of albumin   21367009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of neck   118939000
        Disorder of thyroid gland   14304000
          Inherited disorder of thyroid metabolism   36985004
            Thyroxine transport defect   56112001
              Autosomal dominant variant form of albumin   21367009

ancestors
sorted most to least specific
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