Hereditary amyloidosis   367601000119103

SNOMED CT code


SNOMED code367601000119103
nameHereditary amyloidosis
statusactive
date introduced2017-07-31
fully specified name(s)Hereditary amyloidosis (disorder)
synonymsHereditary amyloidosis
attributes - group1
Associated morphologyAmyloid deposition   68790008
parents
children
  • AGel amyloidosis   783160006
  • Autosomal dominant beta2-microglobulinic amyloidosis   722292000
  • Familial amyloid nephropathy with urticaria AND deafness   15123008
  • Familial amyloid polyneuropathy   42295001
  • Gelatinous droplike corneal dystrophy   419900000
  • Hereditary cerebrovascular amyloidosis   237867001
  • Hereditary oculoleptomeningeal amyloid angiopathy   43532007
  • Hereditary systemic amyloidosis   107311000119104
  • Heredofamilial systemic amyloidosis affecting skin   402459005
  • ITM2B-related amyloidosis   1187126002
  • Lattice corneal dystrophy Type II   419087002  removed: 2020-01-31
  • Localized hereditary amyloidosis   237869003
  • Prion protein systemic amyloidosis   733422008
  • Transthyretin related familial amyloid cardiomyopathy   715655000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Amyloidosis   17602002
          Hereditary amyloidosis   367601000119103

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary amyloidosis   367601000119103

ancestors
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