1197057002: Hallermann Streiff like syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\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\Hallermann Streiff like syndrome

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

\Musculoskeletal finding\Disorder of musculoskeletal system\...

\Disorder of skeletal system\Congenital skeletal dysplasia\Hallermann Streiff like syndrome

\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Hallermann Streiff like syndrome

\Disease\Genetic disease\Hallermann Streiff like syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Hallermann Streiff like syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Hallermann Streiff like syndrome
\Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Hallermann Streiff like syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Hallermann Streiff like syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Hallermann Streiff like syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Hallermann Streiff like syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Hallermann Streiff like syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Hallermann Streiff like syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Hallermann Streiff like syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Hallermann Streiff like syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

4694760013 Dennis Fairhurst Moore syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

4694761012 Hallermann Streiff like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

4694762017 Hallermann Streiff like syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

4694763010 Hallermann Streiff François syndrome severe form en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hallermann Streiff like syndrome	Is a	Congenital skeletal dysplasia	true	Inferred relationship	Existential restriction modifier
Hallermann Streiff like syndrome	Is a	Multiple malformation syndrome with facial defects as major feature	true	Inferred relationship	Existential restriction modifier
Hallermann Streiff like syndrome	Is a	Genetic disease	true	Inferred relationship	Existential restriction modifier
Hallermann Streiff like syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Hallermann Streiff like syndrome	Finding site	Skeletal system structure	true	Inferred relationship	Existential restriction modifier	1
Hallermann Streiff like syndrome	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Hallermann Streiff like syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Hallermann Streiff like syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Hallermann Streiff like syndrome	Finding site	Face structure	true	Inferred relationship	Existential restriction modifier	2
Hallermann Streiff like syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2
Hallermann Streiff like syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2

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
4694760013	Dennis Fairhurst Moore syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
4694761012	Hallermann Streiff like syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
4694762017	Hallermann Streiff like syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
4694763010	Hallermann Streiff François syndrome severe form	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module