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:

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

1997401000052116 Hanharts syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

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	kongenital anomali	false	Inferred relationship	Some	1
Hanhart's syndrome	Associated morphology	medfödd missbildning	false	Inferred relationship	Some	1
Hanhart's syndrome	Associated morphology	medfödd missbildning	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	utvecklingsabnormitet	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