Pseudohypoparathyroidism type I A   58833000

SNOMED CT code


SNOMED code58833000
namePseudohypoparathyroidism type I A
statusactive
date introduced2002-01-31
fully specified name(s)Pseudohypoparathyroidism type I A (disorder)
synonyms
  • Pseudohypoparathyroidism type 1A
  • AHO - Albright hereditary osteodystrophy
  • Albright hereditary osteodystrophy
  • Pseudohypoparathyroidism type Ia
  • Pseudohypoparathyroidism type I A
  • Albright hereditary osteodystrophy, classical type
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteBone structure   272673000
Associated morphologyDysplasia   25723000
attributes - group2
InterpretsHormone secretion   60877009
Has interpretationDecreased   1250004
attributes - group3
Finding siteParathyroid structure   111002
OccurrenceCongenital   255399007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Acromesomelic dysplasia syndrome   279082008
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of endocrine system   363104002
  • Hereditary disorder of musculoskeletal system   363212003
  • Metabolic bone disease   50279003
  • Pseudohypoparathyroidism   58976002
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
              Pseudohypoparathyroidism type I A   58833000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Acromesomelic dysplasia syndrome   279082008
              Pseudohypoparathyroidism type I A   58833000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Pseudohypoparathyroidism type I A   58833000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Hereditary disorder of endocrine system   363104002
            Pseudohypoparathyroidism type I A   58833000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Pseudohypoparathyroidism type I A   58833000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic bone disease   50279003
          Pseudohypoparathyroidism type I A   58833000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Endocrine finding   106176003
      Decreased hormone secretion   42497006
        Hypoparathyroidism   36976004
          Pseudohypoparathyroidism   58976002
            Pseudohypoparathyroidism type I A   58833000

ancestors
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