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 |
3305066017 | This syndrome is extremely rare and has characteristics of delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. To date, six cases have been reported in five families. Dysmorphic features include asymmetrical face, unilateral narrow palpebral fissure, divergent strabismus, long philtrum, high-arched palate, apparently low-set ears and transverse ear lobe creases on both sides. Delayed language development is constant but intellectual development can be normal. In one family, the transmission was compatible with either autosomal dominant or X-linked dominant inheritance. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401265019 | This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401266018 | This syndrome is extremely rare and is characterised by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3305063013 | Delayed speech and facial asymmetry with strabismus and ear lobe skin crease syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3305064019 | Delayed speech and facial asymmetry with strabismus and ear lobe skin crease syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3305065018 | Mehes syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Is a | Hereditary disease | false | Inferred relationship | Some | ||
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Is a | Speech delay | true | Inferred relationship | Some | ||
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Associated morphology | dysgenese | false | Inferred relationship | Some | 1 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Interprets | Ability to perform functions related to communication | true | Inferred relationship | Some | 2 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Interprets | Speech and language observable | false | Inferred relationship | Some | 3 | |
This syndrome is extremely rare and is characterized by delayed speech development, mild facial asymmetry, strabismus and transverse ear lobe creases. | Is a | Developmental hereditary 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)