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720599002: Campomelia Cumming type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5402420011 Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402421010 Campomelia, Cumming type, is characterised by the association of limb defects and multivisceral anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321490013 Campomelia Cumming type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321491012 Campomelia Cumming type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321492017 Cumming syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
947081000172116 campomélie type Cumming fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3420441001000114 Kampomelie Typ Cumming de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology Lymphatic edema true Inferred relationship Some 3
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Congenital anomaly of limb true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Hereditary lymphedema false Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a déformation d'un os false Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Bent bone dysplasia group true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Connective tissue hereditary disorder false Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Deformity of limb (finding) true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology Congenital abnormal curvature false Inferred relationship Some 4
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Occurrence Congenital false Inferred relationship Some 4
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Finding site Bone structure of limb false Inferred relationship Some 4
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology Congenital dysplasia false Inferred relationship Some 5
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Occurrence Congenital false Inferred relationship Some 5
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Finding site Bone structure false Inferred relationship Some 5
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Occurrence Congenital true Inferred relationship Some 2
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Occurrence Congenital true Inferred relationship Some 1
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Finding site Bone structure of limb true Inferred relationship Some 2
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology Congenital dysplasia false Inferred relationship Some 1
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Finding site Bone structure true Inferred relationship Some 1
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology Congenital abnormal curvature true Inferred relationship Some 2
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Congenital deformity false Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Associated morphology Dysplasia true Inferred relationship Some 1
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Developmental hereditary disorder true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Lymphedema true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Deformation of bone true Inferred relationship Some
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. Is a Congenital deformity of musculoskeletal system (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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