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59763006: Hyperphosphatasemia tarda (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
498534010 Van Buchem disease en Synonym Active Case sensitive SNOMED CT core
498535011 Hyperphosphatasaemia tarda en Synonym Active Case insensitive SNOMED CT core
798641018 Hyperphosphatasemia tarda (disorder) en Fully specified name Active Case insensitive SNOMED CT core
99274013 Hyperphosphatasemia tarda en Synonym Active Case insensitive SNOMED CT core
99275014 Hyperostosis corticalis generalisata en Synonym Active Case insensitive SNOMED CT core
99276010 Leontiasis ossea generalisata en Synonym Active Case insensitive SNOMED CT core
99277018 Hyperphosphatasia tarda en Synonym Active Case insensitive SNOMED CT core
99278011 van Buchem's syndrome en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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