Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3722889019 | Macrosomia, microphthalmia, cleft palate syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3722890011 | Teebi Al Saleh Hassoon syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3722891010 | Macrosomia, microphthalmia, cleft palate syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3722892015 | A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of early macrosomia, bilateral severe microphthalmia and a protuberant abdomen with hepatomegaly. Additional reported features include brachycephaly, large fontanelles, prominent forehead, upturned nose and median cleft palate. Cyanotic apneic spells and overwhelming infection lead to death within the first 6 months of life. There have been no further descriptions in the literature since 1989. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3722893013 | A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of early macrosomia, bilateral severe microphthalmia and a protuberant abdomen with hepatomegaly. Additional reported features include brachycephaly, large fontanelles, prominent forehead, upturned nose and median cleft palate. Cyanotic apnoeic spells and overwhelming infection lead to death within the first 6 months of life. There have been no further descriptions in the literature since 1989. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Macrosomia, microphthalmia, cleft palate syndrome | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Macrosomia, microphthalmia, cleft palate syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Macrosomia, microphthalmia, cleft palate syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Macrosomia, microphthalmia, cleft palate syndrome | Finding site | øje som helhed | false | Inferred relationship | Some | 1 | |
Macrosomia, microphthalmia, cleft palate syndrome | Is a | Microphthalmos | true | Inferred relationship | Some | ||
Macrosomia, microphthalmia, cleft palate syndrome | Associated morphology | Congenital smallness | true | Inferred relationship | Some | 1 | |
Macrosomia, microphthalmia, cleft palate syndrome | Is a | Multiple malformation syndrome with early overgrowth | true | Inferred relationship | Some | ||
Macrosomia, microphthalmia, cleft palate syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Macrosomia, microphthalmia, cleft palate syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Macrosomia, microphthalmia, cleft palate syndrome | Finding site | Entire eye proper | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets