35031005: Hanhart's syndrome (disorder)

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

\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Hanhart's syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Hanhart's syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Hanhart's syndrome

\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Hanhart's syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Hanhart's syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Hanhart's syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Hanhart's syndrome
\Disease\Developmental disorder\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Hanhart's syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Hanhart's syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Hanhart's syndrome

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
Hanhart's syndrome	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Some
Hanhart's syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Some
Hanhart's syndrome	Finding site	Bone structure	false	Inferred relationship	Some	1
Hanhart's syndrome	Occurrence	Congenital	false	Inferred relationship	Some
Hanhart's syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Hanhart's syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Some	1
Hanhart's syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Some	1
Hanhart's syndrome	Finding site	Bone structure	false	Inferred relationship	Some	1
Hanhart's syndrome	Occurrence	Congenital	false	Inferred relationship	Some	2
Hanhart's syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	2
Hanhart's syndrome	Finding site	Bone structure	false	Inferred relationship	Some	2
Hanhart's syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Hanhart's syndrome	Finding site	Bone structure	true	Inferred relationship	Some	1
Hanhart's syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Hanhart's syndrome	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
58452016	Hanhart's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
58453014	Micrognathia with peromelia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
766625015	Hanhart's syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2840245012	Hanhart syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5553361000172114	syndrome de micrognathie et péromélie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5553391000172116	syndrome de Hanhart	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
5553401000172119	syndrome d'hypoglossie et hypodactylie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5553371000172117	Hanhart-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
5553381000172119	syndroom van micrognathie met malformatie van extremiteit	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5553411000172116	syndroom van Hanhart	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
5553421000172114	syndroom van micrognathie met peromelie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
7691131000172117	syndroom van micrognathie met malformatie van lidmaat	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)