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59763006: Hyperphosphatasemia tarda (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Mass of body structure\Mass of musculoskeletal structure (finding)\Exostosis (disorder)\Hyperphosphatasemia tarda

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

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

Descriptions:

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 (core metadata concept)
Hyperphosphatasemia tarda	Is a	Congenital anomaly of skull	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Is a	Congenital anomaly of cartilage	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Is a	Metabolic bone disease (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Is a	Endosteal hyperostoses (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Is a	Leontiasis ossium	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Associated morphology	Dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Finding site	Cartilaginous tissue structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Causative agent (attribute)	Mycobacterium leprae (organism)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Finding site	Subcutaneous tissue structure of face	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Associated morphology	Leonine facies (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Associated morphology	Hypertrophy of bone	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Finding site	Bone structure of cranium	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Pathological process	Infectious disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Associated morphology	Abnormally hard consistency	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Is a	Congenital anomaly of face	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Has definitional manifestation	Leonine facies (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Is a	Congenital anomaly of integument	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Is a	Congenital bacterial disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Is a	Hypertrophy of bone (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Finding site	Bone structure of cranium	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Associated morphology	Hypertrophy of bone	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Associated morphology	Hypertrophy of bone	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Finding site	Endosteum	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Finding site	Endosteum	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hyperphosphatasemia tarda	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hyperphosphatasemia tarda	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hyperphosphatasemia tarda	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hyperphosphatasemia tarda	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Is a	Exostosis (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperphosphatasemia tarda	Associated morphology	External hyperostosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperphosphatasemia tarda	Clinical course	Progressive	true	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Hyperphosphatasemia tarda	Interprets	Osteoclast turnover rate	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hyperphosphatasemia tarda	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hyperphosphatasemia tarda	Interprets	Bone density scan	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperphosphatasemia tarda	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	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 (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
99274013	Hyperphosphatasemia tarda	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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	Only initial character 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
498533016	Endosteal hyperostosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
498534010	Van Buchem disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (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	Only initial character case insensitive (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	Only initial character 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
3395921001000115	Hyperostosis corticalis generalisata	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
203131000077112	hyperphosphatasemia tarda	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
203131000077112	hyperphosphatasemia tarda	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3395921001000115	Hyperostosis corticalis generalisata	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module