Metabolic bone disease   50279003

SNOMED CT code


SNOMED code50279003
nameMetabolic bone disease
statusactive
date introduced2002-01-31
fully specified name(s)Metabolic bone disease (disorder)
synonyms
  • Metabolic disorder of bone
  • Metabolic bone disease
attributes - group1
Finding siteBone structure   272673000
parents
children
  • Acroosteolysis, keloid-like lesions, premature aging syndrome   776417008
  • Autosomal dominant hypophosphatemic bone disease   237890006
  • Autosomal recessive cutis laxa type 2A   784381008
  • Autosomal recessive cutis laxa type 2B   778068007
  • Brachytelephalangic chondrodysplasia punctata   778067002
  • Brown tumor of hyperparathyroidism   203471008
  • Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome   1220595008
  • Chondrodysplasia punctata, X-linked dominant type   398958000
  • Craniofaciofrontodigital syndrome   763320005
  • Cutis laxa with osteodystrophy   73856006
  • Cutis laxa, x-linked   59399004
  • Desmosterolosis   709490002
  • Disorder with defective osteoid mineralization   126533001
  • Dysostosis multiplex group   279081001
  • Ehlers-Danlos syndrome   2300005  removed: 2003-07-31
  • Ehlers-Danlos syndrome   398114001
  • Geroderma osteodysplastica   254116003
  • Hepatic osteodystrophy   28193003
  • Hungry bones syndrome   237883001
  • Hyperphosphatasemia with bone disease   9723006
  • Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome   770755007
  • Jarcho-Levin syndrome   61367005
  • Larsen-like syndrome B3GAT3 type   763778003
  • Mandibular hypoplasia, deafness, progeroid syndrome   773406003
  • Menkes kinky-hair syndrome   59178007
  • Metabolic bone disease of prematurity   722928002
  • Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria   724146008
  • Morquio syndrome   378007
  • Nestor Guillermo progeria syndrome   773331001
  • Osteitis fibrosa cystica   84727000
  • Osteopetrosis with renal tubular acidosis   254122007
  • Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome   722207000
  • Pseudohypoparathyroidism type I A   58833000
  • Rhizomelic chondrodysplasia punctata syndrome   56692003
  • Skeletal fluorosis   240168009
  • Stewart-Morel-Morgagni syndrome   782167001
  • Temtamy preaxial brachydactyly syndrome   777998000
  • Toxic diffuse goiter with acropachy   15470004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic bone disease   50279003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Bone finding   118953000
        Disorder of bone   76069003
          Metabolic bone disease   50279003

ancestors
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