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59763006: hyperostosis corticalis generalisata (aandoening)


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
99274013 Hyperphosphatasemia tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
99275014 Hyperostosis corticalis generalisata en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
99276010 Leontiasis ossea generalisata en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
99277018 Hyperphosphatasia tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
99278011 van Buchem's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
498534010 Van Buchem disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
498535011 Hyperphosphatasaemia tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
798641018 Hyperphosphatasemia tarda (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1457001000146118 hyperostosis corticalis generalisata (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
1457011000146116 hyperostosis corticalis generalisata nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
2573501000146110 ziekte van Van Buchem nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperphosphatasemia tarda Is a Congenital anomaly of integument false Inferred relationship Some
Hyperphosphatasemia tarda Is a Congenital anomaly of skull false Inferred relationship Some
Hyperphosphatasemia tarda Is a Congenital anomaly of cartilage false Inferred relationship Some
Hyperphosphatasemia tarda Is a Metabolic bone disease false Inferred relationship Some
Hyperphosphatasemia tarda Is a Endosteal hyperostoses true Inferred relationship Some
Hyperphosphatasemia tarda Is a Leontiasis ossium false Inferred relationship Some
Hyperphosphatasemia tarda Associated morphology Dysplasia false Inferred relationship Some 1
Hyperphosphatasemia tarda Finding site Skeletal system structure false Inferred relationship Some 1
Hyperphosphatasemia tarda Finding site structuur van cartilago (lichaamsstructuur) false Inferred relationship Some
Hyperphosphatasemia tarda Causative agent Mycobacterium leprae false Inferred relationship Some
Hyperphosphatasemia tarda Finding site Subcutaneous tissue structure of face false Inferred relationship Some
Hyperphosphatasemia tarda Associated morphology Leonine facies false Inferred relationship Some 2
Hyperphosphatasemia tarda Associated morphology hypertrofie van bot (afwijkende morfologie) false Inferred relationship Some 2
Hyperphosphatasemia tarda Finding site Bone structure of cranium false Inferred relationship Some 2
Hyperphosphatasemia tarda Finding site Skin structure false Inferred relationship Some
Hyperphosphatasemia tarda Finding site Bone structure false Inferred relationship Some 1
Hyperphosphatasemia tarda Occurrence Congenital false Inferred relationship Some
Hyperphosphatasemia tarda Pathological process Infectious disease false Inferred relationship Some
Hyperphosphatasemia tarda Associated morphology Abnormally hard consistency false Inferred relationship Some
Hyperphosphatasemia tarda Is a Congenital anomaly of face false Inferred relationship Some
Hyperphosphatasemia tarda Has definitional manifestation Leonine facies false Inferred relationship Some
Hyperphosphatasemia tarda Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 2
Hyperphosphatasemia tarda Is a Congenital anomaly of integument false Inferred relationship Some
Hyperphosphatasemia tarda Associated morphology Congenital malformation false Inferred relationship Some
Hyperphosphatasemia tarda Is a Congenital bacterial disorder (disorder) false Inferred relationship Some
Hyperphosphatasemia tarda Is a Hypertrophy of bone false Inferred relationship Some
Hyperphosphatasemia tarda Finding site Bone structure of cranium false Inferred relationship Some 2
Hyperphosphatasemia tarda Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 2
Hyperphosphatasemia tarda Associated morphology hypertrofie van bot (afwijkende morfologie) false Inferred relationship Some 1
Hyperphosphatasemia tarda Finding site Bone structure false Inferred relationship Some 2
Hyperphosphatasemia tarda Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 2
Hyperphosphatasemia tarda Associated morphology hypertrofie van bot (afwijkende morfologie) false Inferred relationship Some 1
Hyperphosphatasemia tarda Finding site Endosteum false Inferred relationship Some 1
Hyperphosphatasemia tarda Finding site Bone structure false Inferred relationship Some 2
Hyperphosphatasemia tarda Finding site Endosteum true Inferred relationship Some 1
Hyperphosphatasemia tarda Occurrence Congenital true Inferred relationship Some 3
Hyperphosphatasemia tarda Finding site Bone structure true Inferred relationship Some 3
Hyperphosphatasemia tarda Associated morphology Dysplasia true Inferred relationship Some 3
Hyperphosphatasemia tarda Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 3
Hyperphosphatasemia tarda Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hyperphosphatasemia tarda Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Hyperphosphatasemia tarda Occurrence Congenital false Inferred relationship Some 2
Hyperphosphatasemia tarda Is a Exostosis (disorder) true Inferred relationship Some
Hyperphosphatasemia tarda Associated morphology External hyperostosis true Inferred relationship Some 1
Hyperphosphatasemia tarda Clinical course Progressive (qualifier value) true Inferred relationship Some 5
Hyperphosphatasemia tarda Interprets Osteoclast turnover rate true Inferred relationship Some 4
Hyperphosphatasemia tarda Has interpretation Above reference range true Inferred relationship Some 2
Hyperphosphatasemia tarda Has interpretation Below reference range true Inferred relationship Some 4
Hyperphosphatasemia tarda Interprets Bone density scan true Inferred relationship Some 2
Hyperphosphatasemia tarda Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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