Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3724878013 | Frontonasal dysplasia type 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3724879017 | ALX1-related frontonasal dysplasia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3724880019 | Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3724881015 | ALX1 (aristaless-like homeobox 1) related frontonasal dysplasia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3724882010 | Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Finding site | Face structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Cleft palate | true | Inferred relationship | Existential restriction modifier | ||
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Digestive system hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 3 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Microphthalmos | true | Inferred relationship | Existential restriction modifier | ||
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 2 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Finding site | Bone structure of cranium | true | Inferred relationship | Existential restriction modifier | 4 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 4 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Finding site | Palatal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Associated morphology | Congenital dysplasia | false | Inferred relationship | Existential restriction modifier | 4 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Finding site | Entire eye | true | Inferred relationship | Existential restriction modifier | 3 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 3 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Associated morphology | Developmental failure of fusion | true | Inferred relationship | Existential restriction modifier | 1 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Associated morphology | Congenital smallness | true | Inferred relationship | Existential restriction modifier | 3 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 4 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Frontonasal dysplasia sequence | true | Inferred relationship | Existential restriction modifier | ||
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Associated morphology | Dysplasia | true | Inferred relationship | Existential restriction modifier | 4 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Associated morphology | Developmental failure of fusion | false | Inferred relationship | Existential restriction modifier | 5 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Pathological process | Pathological developmental process | false | Inferred relationship | Existential restriction modifier | 5 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 5 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Finding site | Bone structure of head | false | Inferred relationship | Existential restriction modifier | 5 | |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets