59763006: Hyperphosphatasemia tarda (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Imaging finding\Bone densimetry abnormal\Bone density above reference range\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda

\Mass of body structure\Mass of musculoskeletal structure\Exostosis\Hyperphosphatasemia tarda

\General finding of observation of patient\Procedure related finding\Bone density finding\Bone density above reference range\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda

\Musculoskeletal finding\Mass of musculoskeletal structure\Exostosis\Hyperphosphatasemia tarda
\Musculoskeletal finding\Bone finding\Bone density finding\Bone density above reference range\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Bone finding\Disorder of bone\Exostosis\Hyperphosphatasemia tarda
\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Bone finding\Disorder of bone\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Exostosis\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Exostosis\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Chronic disease\Chronic disease of musculoskeletal system\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Developmental disorder\Developmental hereditary disorder\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteochondrodysplasia with osteopetrosis\Endosteal hyperostoses\Hyperphosphatasemia tarda

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

Descriptions:

Id Description Lang Type Status Case? Module

99274013 Hyperphosphatasemia tarda en Synonym Active Entire term case insensitive SNOMED CT core module

99275014 Hyperostosis corticalis generalisata en Synonym Active Entire term case insensitive SNOMED CT core module

99276010 Leontiasis ossea generalisata en Synonym Active Entire term case insensitive SNOMED CT core module

99277018 Hyperphosphatasia tarda en Synonym Active Entire term case insensitive SNOMED CT core module

99278011 van Buchem's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

498534010 Van Buchem disease en Synonym Active Entire term case sensitive SNOMED CT core module

498535011 Hyperphosphatasaemia tarda en Synonym Active Entire term case insensitive SNOMED CT core module

798641018 Hyperphosphatasemia tarda (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

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