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9723006: Hyperphosphatasemia with bone disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
16993011 Hyperphosphatasemia with bone disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16994017 Chronic congenital idiopathic hyperphosphatasemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16995016 Familial idiopathic hyperphosphatasemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16996015 Familial osteoectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16997012 Hyperostosis corticalis deformans juvenilis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16998019 Juvenile Paget disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16999010 Osteochalasia desmalis familiaris en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512746019 Osteoectasia with hyperphosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512747011 Chronic congenital idiopathic hyperphosphatasaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512748018 Hyperphosphatasaemia with bone disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512749014 Familial idiopathic hyperphosphatasaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
841761014 Hyperphosphatasemia with bone disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
16993011 Hyperphosphatasemia with bone disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16993011 Hyperphosphatasemia with bone disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16994017 Chronic congenital idiopathic hyperphosphatasemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16994017 Chronic congenital idiopathic hyperphosphatasemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16995016 Familial idiopathic hyperphosphatasemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16995016 Familial idiopathic hyperphosphatasemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16996015 Familial osteoectasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16996015 Familial osteoectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16997012 Hyperostosis corticalis deformans juvenilis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16997012 Hyperostosis corticalis deformans juvenilis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
16998019 Juvenile Paget disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16999010 Osteochalasia desmalis familiaris en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
16999010 Osteochalasia desmalis familiaris en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512746019 Osteoectasia with hyperphosphatasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
512746019 Osteoectasia with hyperphosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512747011 Chronic congenital idiopathic hyperphosphatasaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
512747011 Chronic congenital idiopathic hyperphosphatasaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512748018 Hyperphosphatasaemia with bone disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
512748018 Hyperphosphatasaemia with bone disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512749014 Familial idiopathic hyperphosphatasaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
512749014 Familial idiopathic hyperphosphatasaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
841761014 Hyperphosphatasemia with bone disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
841761014 Hyperphosphatasemia with bone disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3419011001000116 Paget-Syndrom, juveniles de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4421431000241117 hyperphosphatasémie associée à une maladie osseuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4421431000241117 hyperphosphatasémie associée à une maladie osseuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3419011001000116 Paget-Syndrom, juveniles de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperphosphatasemia with bone disease Is a Disorder of phosphate, calcium and vitamin D metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperphosphatasemia with bone disease Is a Dysplasia with increased bone density true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperphosphatasemia with bone disease Is a Disorder of bone (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hyperphosphatasemia with bone disease Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Associated morphology Hypertrophy of bone false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hyperphosphatasemia with bone disease Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Is a Metabolic bone disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Is a Hypertrophy of bone (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperphosphatasemia with bone disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperphosphatasemia with bone disease Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperphosphatasemia with bone disease Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatasemia with bone disease Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Interprets Bone density scan true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperphosphatasemia with bone disease Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperphosphatasemia with bone disease Finding site Skeletal system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia with bone disease Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Idiopathic hyperphosphatasemia Is a False Hyperphosphatasemia with bone disease Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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