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37068007: Lateral displacement (morphologic abnormality)

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
61837012 Lateral displacement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
61838019 Lateroflexion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768891012 Lateral displacement (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lateral displacement Is a Displacement true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Lateral displacement, right Is a True Lateral displacement Inferred relationship Some
Lateral displacement, left Is a True Lateral displacement Inferred relationship Some
Deviated nasal septum Associated morphology False Lateral displacement Inferred relationship Some 1
Right-sided displacement of abomasum Associated morphology False Lateral displacement Inferred relationship Some 1
Lateral displacement of eye (disorder) Associated morphology False Lateral displacement Inferred relationship Some 1
Left-sided displacement of abomasum Associated morphology False Lateral displacement Inferred relationship Some 1
Congenital deviation of nasal septum Associated morphology True Lateral displacement Inferred relationship Some 1
Acquired deviated nasal septum Associated morphology False Lateral displacement Inferred relationship Some 1
Acquired deviated nasal septum Associated morphology True Lateral displacement Inferred relationship Some 1
Right-sided displacement of abomasum Associated morphology False Lateral displacement Inferred relationship Some 1
Lateral displacement of eye (disorder) Associated morphology True Lateral displacement Inferred relationship Some 1
Deviated nasal septum Associated morphology True Lateral displacement Inferred relationship Some 1
Left-sided displacement of abomasum Associated morphology False Lateral displacement Inferred relationship Some 1
Dystopia canthorum (disorder) Associated morphology True Lateral displacement Inferred relationship Some 1
Columelloplasty Direct morphology True Lateral displacement Inferred relationship Some 1
Congenital radial deviation of finger (disorder) Associated morphology True Lateral displacement Inferred relationship Some 1
Paraspadias Associated morphology False Lateral displacement Inferred relationship Some 1
Congenital bent nose (disorder) Associated morphology True Lateral displacement Inferred relationship Some 1
Nasal deviation Associated morphology True Lateral displacement Inferred relationship Some 1
Nasal deviation, bone Associated morphology True Lateral displacement Inferred relationship Some 1
Nasal deviation, cartilage Associated morphology True Lateral displacement Inferred relationship Some 1
Closed lateral dislocation of proximal end of tibia Associated morphology True Lateral displacement Inferred relationship Some 1
Bilateral congenital radial deviation of fingers Associated morphology True Lateral displacement Inferred relationship Some 1
Bilateral congenital radial deviation of fingers Associated morphology True Lateral displacement Inferred relationship Some 2
A very rare subtype of Waardenburg syndrome (WS) with characteristics of limb anomalies in association with congenital hearing loss, minor defects in structures arising from neural crest, resulting in pigmentation anomalies of eyes, hair, and skin. Caused by heterozygous or homozygous mutations in the PAX3 (2q36.1) gene. Associated morphology True Lateral displacement Inferred relationship Some 5
A subtype of Waardenburg syndrome (WS) with characteristics of congenital deafness, minor defects in structures arising from neural crest resulting in pigmentation anomalies of eyes, hair, and skin, in combination with dystopia canthorum. Caused by a heterozygous mutation in the paired box-containing PAX3 gene on chromosome 2q36.1. In the majority of cases, WS1 is transmitted as an autosomal dominant disorder with a large variable inter and intrafamilial expressivity. Some affected patients present with a de novo mutation. Associated morphology True Lateral displacement Inferred relationship Some 2

This concept is not in any reference sets

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