Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3304688014 | Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304689018 | Short stature with craniofacial anomalies and genital hypoplasia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304695017 | Haspeslagh Fryns Muelenaere syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401213016 | A rare developmental defect during embryogenesis mainly characterized by severe intellectual disability, short stature, hypogonadism, and distinct facial dysmorphism (including trigonocephaly, prominent forehead, asymmetric and flat face, hypertelorism, epicanthus, downslanting palpebral fissures, ptosis, low-set angulated ears, small mouth, high-arched/cleft palate crowded teeth, microretrognathia), as well as slender hands and/or feet. Variable additional features may include pterygia, hypoplastic nipples, cardiac anomaly, distal muscular wasting, limb contractures, skeletal anomalies (e.g. scoliosis, pectus excavatum, bilateral clubfeet), hypothyroidism, seizures, and cerebral anomalies. Puberty may be delayed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401214010 | A rare developmental defect during embryogenesis mainly characterised by severe intellectual disability, short stature, hypogonadism, and distinct facial dysmorphism (including trigonocephaly, prominent forehead, asymmetric and flat face, hypertelorism, epicanthus, downslanting palpebral fissures, ptosis, low-set angulated ears, small mouth, high-arched/cleft palate crowded teeth, microretrognathia), as well as slender hands and/or feet. Variable additional features may include pterygia, hypoplastic nipples, cardiac anomaly, distal muscular wasting, limb contractures, skeletal anomalies (e.g. scoliosis, pectus excavatum, bilateral clubfeet), hypothyroidism, seizures, and cerebral anomalies. Puberty may be delayed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Congenital malformation of genital organs (disorder) | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Short stature disorder | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Congenital abnormality of skull and face bones | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 3 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 5 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Finding site | Bone structure of head | false | Inferred relationship | Some | 5 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 4 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Finding site | Face structure | false | Inferred relationship | Some | 4 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Associated morphology | Congenital hypoplasia | false | Inferred relationship | Some | 3 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Finding site | Genital structure | false | Inferred relationship | Some | 3 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Finding site | Bone structure of head | true | Inferred relationship | Some | 2 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Finding site | Genital structure | true | Inferred relationship | Some | 1 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) | Interprets | Height / growth measure | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)