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74370006: Micromelia (disorder)

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

\Finding by site\Finding of body region\Finding of limb structure\Disorder of extremity (disorder)\Congenital anomaly of limb\Micromelia
\Finding by site\Disorder by body site (disorder)\Disorder of extremity (disorder)\Congenital anomaly of limb\Micromelia

\Disease\Disorder by body site (disorder)\Disorder of extremity (disorder)\Congenital anomaly of limb\Micromelia
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of limb\Micromelia
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of limb\Micromelia

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module	Reference Sets
123510010	Micromelia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	GB English: Preferred (foundation metadata concept)
123512019	Micromelus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	GB English: Acceptable (foundation metadata concept)
123513012	Micromelic dwarf	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	GB English: Acceptable (foundation metadata concept)
123515017	Nanomelia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	GB English: Acceptable (foundation metadata concept)
814861012	Micromelia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	GB English: Preferred (foundation metadata concept)
2007791000052113	mikromeli	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)	Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Micromelia	Is a	Longitudinal deficiency of limb	false	Inferred relationship	Some
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Associated morphology	Developmental anomaly (morphologic abnormality)	false	Inferred relationship	Some
Micromelia	Associated morphology	Congenital smallness	false	Inferred relationship	Some	1
Micromelia	Associated morphology	Abnormally short growth	false	Inferred relationship	Some	2
Micromelia	Finding site	Musculoskeletal structure of limb	false	Inferred relationship	Some
Micromelia	Occurrence	Congenital	false	Inferred relationship	Some
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	2
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	2
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	2
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	2
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	2
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	2
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	1
Micromelia	Associated morphology	Congenital smallness	true	Inferred relationship	Some	1
Micromelia	Occurrence	Congenital	false	Inferred relationship	Some	2
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	2
Micromelia	Associated morphology	Abnormally short growth	false	Inferred relationship	Some	2
Micromelia	Occurrence	Congenital	false	Inferred relationship	Some	3
Micromelia	Associated morphology	Abnormal shortening	false	Inferred relationship	Some	3
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	3
Micromelia	Associated morphology	Abnormal shortening	false	Inferred relationship	Some	2
Micromelia	Is a	Congenital anomaly of limb	true	Inferred relationship	Some
Micromelia	Finding site	Entire limb	false	Inferred relationship	Some	2
Micromelia	Associated morphology	Congenital smallness	false	Inferred relationship	Some	4
Micromelia	Occurrence	Congenital	false	Inferred relationship	Some	4
Micromelia	Finding site	Limb structure	false	Inferred relationship	Some	4
Micromelia	Occurrence	Congenital	true	Inferred relationship	Some	1
Micromelia	Finding site	Entire limb	true	Inferred relationship	Some	1
Micromelia	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Microlissencephaly micromelia syndrome (disorder)	Is a	True	Micromelia	Inferred relationship	Some
Short rib polydactyly syndrome type I (disorder)	Is a	True	Micromelia	Inferred relationship	Some
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)	Is a	True	Micromelia	Inferred relationship	Some
Diastrophic dysplasia	Is a	True	Micromelia	Inferred relationship	Some
Micromelic dwarfism Fryn type	Is a	True	Micromelia	Inferred relationship	Some

This concept is not in any reference sets

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