14870002: Achondrogenesis, type IB (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of general physiological development\Disorder of stature\Short stature disorder\Congenital malformation syndromes associated with short stature\Achondrogenesis\Achondrogenesis, type IB

\General finding of observation of patient\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Short stature disorder\Congenital malformation syndromes associated with short stature\Achondrogenesis\Achondrogenesis, type IB

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Achondrogenesis, type IB
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Achondrogenesis\Achondrogenesis, type IB
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Achondrogenesis, type IB
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Achondrogenesis\Achondrogenesis, type IB
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Achondrogenesis, type IB

\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Achondrogenesis\Achondrogenesis, type IB
\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\Achondrogenesis, type IB
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Achondrogenesis\Achondrogenesis, type IB
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Achondrogenesis, type IB
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Congenital malformation syndromes associated with short stature\Achondrogenesis\Achondrogenesis, type IB
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Achondrogenesis\Achondrogenesis, type IB
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Achondrogenesis, type IB
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Achondrogenesis, type IB
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Congenital malformation syndromes associated with short stature\Achondrogenesis\Achondrogenesis, type IB
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Achondrogenesis\Achondrogenesis, type IB
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Achondrogenesis, type IB
\Disease\Developmental disorder\Disorder of stature\Short stature disorder\Congenital malformation syndromes associated with short stature\Achondrogenesis\Achondrogenesis, type IB

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

25257011 Achondrogenesis, type IB en Synonym Active Only initial character case insensitive SNOMED CT core module

741311019 Achondrogenesis, type IB (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Achondrogenesis, type IB	Is a	Achondrogenesis	true	Inferred relationship	Existential restriction modifier
Achondrogenesis, type IB	Finding site	Both upper extremities	false	Inferred relationship	Existential restriction modifier
Achondrogenesis, type IB	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Achondrogenesis, type IB	Finding site	Both lower extremities	false	Inferred relationship	Existential restriction modifier
Achondrogenesis, type IB	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Achondrogenesis, type IB	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	2
Achondrogenesis, type IB	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Achondrogenesis, type IB	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Achondrogenesis, type IB	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Achondrogenesis, type IB	Associated morphology	Congenital hypoplasia	false	Inferred relationship	Existential restriction modifier	3
Achondrogenesis, type IB	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	3
Achondrogenesis, type IB	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Achondrogenesis, type IB	Associated morphology	Hypoplasia	true	Inferred relationship	Existential restriction modifier	1
Achondrogenesis, type IB	Finding site	Skeletal system structure	true	Inferred relationship	Existential restriction modifier	2
Achondrogenesis, type IB	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier
Achondrogenesis, type IB	Interprets	Height / growth measure	true	Inferred relationship	Existential restriction modifier	3

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
25257011	Achondrogenesis, type IB	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
741311019	Achondrogenesis, type IB (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module