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 |
3315146015 | X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3315147012 | X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3315148019 | Prieto Badia Mulas syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
6956871000146116 | syndroom van Prieto-Badia-Mulas | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6956881000146119 | X-gebonden syndroom van mentale retardatie, dysmorfie en cerebrale atrofie | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
7495761000146117 | X-gebonden syndroom van verstandelijke beperking, dysmorfie en cerebrale atrofie (aandoening) | nl | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
7719321000146115 | X-gebonden syndroom van verstandelijke beperking, dysmorfie en cerebrale atrofie | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
7869011000146112 | X-gebonden syndroom van verstandelijke handicap, dysmorfie en cerebrale atrofie | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3315149010 | This syndrome has characteristics of intellectual deficit associated with facial dysmorphism, patella luxation and abnormal growth of the teeth. It has been described in eight males from multiple generations of one family. The locus for the causative gene for this syndrome has been located to the region between p11.22 and p21.1 on the X chromosome. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | Multiple malformation syndrome with facial-limb defects as major feature | true | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | mentale retardatie | false | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | Cerebral atrophy | true | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Associated morphology | gebrekkige ontwikkeling (afwijkende morfologie) | false | Inferred relationship | Some | 5 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Associated morphology | gebrekkige ontwikkeling (afwijkende morfologie) | false | Inferred relationship | Some | 3 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Associated morphology | Atrophy | false | Inferred relationship | Some | 4 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Finding site | Cerebrum | false | Inferred relationship | Some | 4 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Finding site | Limb structure | true | Inferred relationship | Some | 3 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Finding site | Face structure | false | Inferred relationship | Some | 5 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Finding site | Cerebrum | true | Inferred relationship | Some | 2 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 4 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 5 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) | Is a | Congenital neurological disorder (disorder) | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets