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733037000: German syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Deformity\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\German syndrome
\Deformity\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\German syndrome

\Finding of limb structure\Edema of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\German syndrome
\Finding of limb structure\Disorder of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\German syndrome

\Edema\Edema of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\German syndrome
\Edema\Disorder characterized by edema\Lymphedema\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\German syndrome

\Finding of head and neck region\Head finding\...

\Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\German syndrome

\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\German syndrome
\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\German syndrome

\Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\German syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Hereditary lymphedema\German syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Inherited arthrogryposis\German syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\German syndrome
\Disease\Disorder of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\German syndrome
\Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\German syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\German syndrome
\Disease\Disorder characterized by edema\Lymphedema\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\German syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\German syndrome
\Disease\Congenital disease\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\German syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\German syndrome
\Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\German syndrome
\Disease\Developmental disorder\Primary lymphedema\Hereditary lymphedema\German syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Hereditary lymphedema\German syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Inherited arthrogryposis\German syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\German syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\German syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\German syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

3498620010 German syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3498621014 German syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
German syndrome	Is a	Inherited arthrogryposis	true	Inferred relationship	Existential restriction modifier
German syndrome	Is a	Multiple malformation syndrome with facial defects as major feature	true	Inferred relationship	Existential restriction modifier
German syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
German syndrome	Is a	Hereditary lymphedema	true	Inferred relationship	Existential restriction modifier
German syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	4
German syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	5
German syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	5
German syndrome	Finding site	Joint structure	false	Inferred relationship	Existential restriction modifier	5
German syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	6
German syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	7
German syndrome	Finding site	Joint structure	false	Inferred relationship	Existential restriction modifier	7
German syndrome	Associated morphology	Lymphatic edema	true	Inferred relationship	Existential restriction modifier	4
German syndrome	Associated morphology	Contracture	false	Inferred relationship	Existential restriction modifier	7
German syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	6
German syndrome	Finding site	Face structure	false	Inferred relationship	Existential restriction modifier	6
German syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	1
German syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	3
German syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
German syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	3
German syndrome	Associated morphology	Contracture	false	Inferred relationship	Existential restriction modifier	1
German syndrome	Finding site	Face structure	true	Inferred relationship	Existential restriction modifier	3
German syndrome	Finding site	Joint structure	false	Inferred relationship	Existential restriction modifier	1
German syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	1
German syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
German syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
German syndrome	Associated morphology	Contracture	true	Inferred relationship	Existential restriction modifier	2
German syndrome	Has interpretation	Decreased	true	Inferred relationship	Existential restriction modifier	1
German syndrome	Interprets	Range of joint movement	true	Inferred relationship	Existential restriction modifier	1
German syndrome	Finding site	Structure of joint region	true	Inferred relationship	Existential restriction modifier	2
German syndrome	Finding site	Limb structure	true	Inferred relationship	Existential restriction modifier	4
German syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	4

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
3498620010	German syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3498621014	German syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module