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32985001: Greig cephalopolysyndactyly syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Greig cephalopolysyndactyly syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Greig cephalopolysyndactyly syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Greig cephalopolysyndactyly syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Greig cephalopolysyndactyly syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Greig cephalopolysyndactyly syndrome

\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Greig cephalopolysyndactyly syndrome
\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\Greig cephalopolysyndactyly syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Greig cephalopolysyndactyly syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Greig cephalopolysyndactyly syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Greig cephalopolysyndactyly syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Greig cephalopolysyndactyly syndrome
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Greig cephalopolysyndactyly syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Greig cephalopolysyndactyly syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Greig cephalopolysyndactyly syndrome

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

55063010 Greig cephalopolysyndactyly syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

764332017 Greig cephalopolysyndactyly syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Greig cephalopolysyndactyly syndrome	Is a	Congenital skeletal dysplasia	true	Inferred relationship	Existential restriction modifier
Greig cephalopolysyndactyly syndrome	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Greig cephalopolysyndactyly syndrome	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Greig cephalopolysyndactyly syndrome	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Greig cephalopolysyndactyly syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Greig cephalopolysyndactyly syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Greig cephalopolysyndactyly syndrome	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier

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
55063010	Greig cephalopolysyndactyly syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
764332017	Greig cephalopolysyndactyly syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module