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1230271002: Congenital deformity of upper limb (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5068607016 Congenital deformity of upper limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068608014 Congenital deformity of upper limb (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

141 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital deformity of upper limb Is a Congenital deformity true Inferred relationship Some
Congenital deformity of upper limb Is a Deformity of upper limb true Inferred relationship Some
Congenital deformity of upper limb Is a Congenital anomaly of upper limb true Inferred relationship Some
Congenital deformity of upper limb Occurrence Congenital true Inferred relationship Some 1
Congenital deformity of upper limb Finding site Upper extremity, including shoulder, arm, forearm, wrist, and hand true Inferred relationship Some 1
Congenital deformity of upper limb Associated morphology Deformity true Inferred relationship Some 1
Congenital deformity of upper limb Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital cubitus varus Is a True Congenital deformity of upper limb Inferred relationship Some
Congenital cubitus valgus Is a True Congenital deformity of upper limb Inferred relationship Some
Constriction ring syndrome of upper limb Is a True Congenital deformity of upper limb Inferred relationship Some
Longitudinal deficiency of part of upper limb (disorder) Is a True Congenital deformity of upper limb Inferred relationship Some
Reduction deformity of upper limb Is a True Congenital deformity of upper limb Inferred relationship Some
Congenital deformity of bone of forearm (disorder) Is a True Congenital deformity of upper limb Inferred relationship Some
Congenital deformity of left upper limb (disorder) Is a True Congenital deformity of upper limb Inferred relationship Some
Congenital deformity of right upper limb (disorder) Is a True Congenital deformity of upper limb Inferred relationship Some
Congenital deformity of hand (disorder) Is a True Congenital deformity of upper limb Inferred relationship Some
Correction of upper limb congenital ring constriction band Has focus False Congenital deformity of upper limb Inferred relationship Some 1
Correction of congenital deformity of upper limb Has focus True Congenital deformity of upper limb Inferred relationship Some 2
Congenital deformity of shoulder (disorder) Is a True Congenital deformity of upper limb Inferred relationship Some
Congenital deformity of upper arm Is a True Congenital deformity of upper limb Inferred relationship Some
Correction of obstetric palsy Has focus True Congenital deformity of upper limb Inferred relationship Some 2
L'Episcopo operation for obstetric palsy (procedure) Has focus True Congenital deformity of upper limb Inferred relationship Some 2
Zachary operation for obstetric palsy (procedure) Has focus True Congenital deformity of upper limb Inferred relationship Some 2
Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome is an extremely rare, multiple congenital anomalies/dysmorphic syndrome characterized by micrognathia, a short, webbed neck, hypoplastic nipples and joint contractures (which improve over time) of the knees and elbows. In addition, sloping shoulders, mild to moderate hearing loss, mild speech impairment and facies with hypertelorism, short philtrum and tented upper lip may be associated. Is a True Congenital deformity of upper limb Inferred relationship Some
Congenital dolichostenomelia Is a True Congenital deformity of upper limb Inferred relationship Some

This concept is not in any reference sets

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