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38392006: Congenital abnormal curvature (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
63476013 Congenital abnormal curvature en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
773769012 Congenital abnormal curvature (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital abnormal curvature Is a Congenital malposition false Inferred relationship Some
Congenital abnormal curvature Is a Congenital abnormal shape false Inferred relationship Some
Congenital abnormal curvature Is a Abnormal curvature true Inferred relationship Some
Congenital abnormal curvature Is a Congenital deformity false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital chordee Associated morphology False Congenital abnormal curvature Inferred relationship Some 2
Congenital lateral curvature of penis Associated morphology False Congenital abnormal curvature Inferred relationship Some 5
Congenital leg bone bowing Associated morphology False Congenital abnormal curvature Inferred relationship Some 1
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology False Congenital abnormal curvature Inferred relationship Some 4
Clinodactyly of toe (disorder) Associated morphology True Congenital abnormal curvature Inferred relationship Some 1
Keratosis palmaris et plantaris-clinodactyly syndrome is characterized by the association of palmoplantar keratosis with clinodactyly of the fifth finger. Less than 20 cases have been described in the literature so far, and the majority of reported patients were of Mexican origin. Transmission is autosomal dominant. Associated morphology False Congenital abnormal curvature Inferred relationship Some 4
Correction of clinodactyly Direct morphology True Congenital abnormal curvature Inferred relationship Some 2
Correction of clinodactyly with osteotomy and bone graft Direct morphology True Congenital abnormal curvature Inferred relationship Some 4
Familial isolated clinodactyly of fingers is a rare, genetic, non-syndromic, congenital limb malformation disorder characterized by angulation of a digit in the radio-ulnar (coronal) plane, away from the axis of joint flexion-extension, in several members of a single family with no other associated manifestations. Deviation is usually bilateral and commonly involves the fifth finger. Affected digits present trapezoidal or delta-shaped phalanges on imaging. Associated morphology True Congenital abnormal curvature Inferred relationship Some 1
Severe lateral tibial bowing with short stature is a rare, genetic, primary bent bone dysplasia characterized by significant, uni-/bilateral, lateral tibial bowing localized to the distal two-thirds of the tibia, with respective cortical thickening and thinning of the inner and outer tibial curve, loss of normal trabecular bone, bilateral abnormalities of the tibial epiphyses and growth plates, as well as foot abnormalities, including abnormally high arches. Affected individuals have short stature with absence of other skeletal abnormalities. Associated morphology False Congenital abnormal curvature Inferred relationship Some 1
Congenital bowing of tibia, fibula and femur Associated morphology False Congenital abnormal curvature Inferred relationship Some 1
Congenital bowing of tibia, fibula and femur Associated morphology False Congenital abnormal curvature Inferred relationship Some 2
Congenital lateral curvature of penis Associated morphology False Congenital abnormal curvature Inferred relationship Some 1
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology True Congenital abnormal curvature Inferred relationship Some 2
Keratosis palmaris et plantaris-clinodactyly syndrome is characterized by the association of palmoplantar keratosis with clinodactyly of the fifth finger. Less than 20 cases have been described in the literature so far, and the majority of reported patients were of Mexican origin. Transmission is autosomal dominant. Associated morphology True Congenital abnormal curvature Inferred relationship Some 1
A rare, genetic, congenital limb malformation syndrome characterised by a unique combination of bilateral, symmetrical camptodactyly and clinodactyly of 5th fingers, mesoaxial camptodactyly of toes, and ulnar deviation of 3rd fingers. Additional variable manifestations include bifid toes and severe syndactyly, or synpolydactyly, involving all digits of hands and feet. Associated morphology True Congenital abnormal curvature Inferred relationship Some 2
Clinodactyly of bilateral toes (disorder) Associated morphology True Congenital abnormal curvature Inferred relationship Some 1
Clinodactyly of bilateral toes (disorder) Associated morphology True Congenital abnormal curvature Inferred relationship Some 2
Cornea plana of bilateral corneas (disorder) Associated morphology True Congenital abnormal curvature Inferred relationship Some 1
Cornea plana of bilateral corneas (disorder) Associated morphology True Congenital abnormal curvature Inferred relationship Some 2
Congenital clinodactyly of bilateral fingers (disorder) Associated morphology True Congenital abnormal curvature Inferred relationship Some 1
Congenital clinodactyly of bilateral fingers (disorder) Associated morphology True Congenital abnormal curvature Inferred relationship Some 2
Congenital clinodactyly of finger Associated morphology True Congenital abnormal curvature Inferred relationship Some 1
Congenital clinodactyly of little finger Associated morphology True Congenital abnormal curvature Inferred relationship Some 1

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