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