720599002: Campomelia Cumming type (disorder)

SNOMED CT Concept\Clinical finding\...

\Deformity\Deformity of limb\Campomelia Cumming type
\Deformity\Congenital deformity\Campomelia Cumming type
\Deformity\Deformity of bone\Campomelia Cumming type

\Finding of limb structure\Deformity of limb\Campomelia Cumming type
\Finding of limb structure\Disorder of extremity\Congenital anomaly of limb\Campomelia Cumming type

\Edema\Disorder characterized by edema\Lymphedema\Campomelia Cumming type

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Campomelia Cumming type
\Musculoskeletal finding\Bone finding\Disorder of bone\Deformity of bone\Campomelia Cumming type
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Campomelia Cumming type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Campomelia Cumming type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Campomelia Cumming type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Deformity of bone\Campomelia Cumming type
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Campomelia Cumming type
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Campomelia Cumming type

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Campomelia Cumming type
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Campomelia Cumming type
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Campomelia Cumming type
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Campomelia Cumming type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Campomelia Cumming type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Campomelia Cumming type
\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\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Deformity of bone\Campomelia Cumming type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Disorder of extremity\Congenital anomaly of limb\Campomelia Cumming type
\Disease\Disorder characterized by edema\Lymphedema\Campomelia Cumming type
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Campomelia Cumming type
\Disease\Congenital disease\Congenital malformation\Congenital deformity\Campomelia Cumming type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of limb\Campomelia Cumming type
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Developmental disorder\Developmental hereditary disorder\Campomelia Cumming type
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Campomelia Cumming type
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Campomelia Cumming type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Campomelia Cumming type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of limb\Campomelia Cumming type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3321490013 Campomelia Cumming type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3321491012 Campomelia Cumming type en Synonym Active Only initial character case insensitive SNOMED CT core module

3321492017 Cumming syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Campomelia Cumming type	Associated morphology	Lymphatic edema	true	Inferred relationship	Existential restriction modifier	3
Campomelia Cumming type	Is a	Multiple malformation syndrome with limb defect as major feature	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Congenital anomaly of limb	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Hereditary lymphedema	false	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Deformity of bone	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Bent bone dysplasia group	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Connective tissue hereditary disorder	false	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Deformity of limb	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Associated morphology	Congenital abnormal curvature	false	Inferred relationship	Existential restriction modifier	4
Campomelia Cumming type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	4
Campomelia Cumming type	Finding site	Bone structure of extremity	false	Inferred relationship	Existential restriction modifier	4
Campomelia Cumming type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	5
Campomelia Cumming type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	5
Campomelia Cumming type	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	5
Campomelia Cumming type	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Campomelia Cumming type	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Campomelia Cumming type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Campomelia Cumming type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Campomelia Cumming type	Finding site	Bone structure of extremity	true	Inferred relationship	Existential restriction modifier	2
Campomelia Cumming type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Campomelia Cumming type	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Campomelia Cumming type	Associated morphology	Congenital abnormal curvature	true	Inferred relationship	Existential restriction modifier	2
Campomelia Cumming type	Is a	Congenital deformity	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Campomelia Cumming type	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
Campomelia Cumming type	Is a	Lymphedema	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3321490013	Campomelia Cumming type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3321491012	Campomelia Cumming type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3321492017	Cumming syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module