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 |
3323402016 | Deaf blind hypopigmentation syndrome Yemenite type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3323403014 | Deaf blind hypopigmentation syndrome Yemenite type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3323404015 | Warburg Thomsen syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3323405019 | An exceedingly rare genetic disorder with characteristics of cutaneous pigmentation anomalies, ocular disorders and hearing loss. The syndrome was described in 1990 in two patients from the same Yemenite family. A brother and sister were described as having cutaneous patchy hypo and hyperpigmentation on the trunk and extremities, grey hair, white brows and lashes. Ocular manifestations were microcornea, coloboma and abnormalities of the anterior chamber of the eye. Both patients had severe hearing loss and dental abnormalities. Intelligence was reported to be normal. Their parents were unaffected and possibly consanguineous. The cause of this syndrome has not been determined. The inheritance pattern appears to be autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3777415016 | An exceedingly rare genetic disorder with characteristics of cutaneous pigmentation anomalies, ocular disorders and hearing loss. The syndrome was described in 1990 in two patients from the same Yemenite family. A brother and sister were described as having cutaneous patchy hypo and hyperpigmentation on the trunk and extremities, gray hair, white brows and lashes. Ocular manifestations were microcornea, coloboma and abnormalities of the anterior chamber of the eye. Both patients had severe hearing loss and dental abnormalities. Intelligence was reported to be normal. Their parents were unaffected and possibly consanguineous. The cause of this syndrome has not been determined. The inheritance pattern appears to be autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Congenital deficiency of pigment of skin | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Congenital anomaly of eye | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Finding site | Ear structure | false | Inferred relationship | Some | 3 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Associated morphology | dysgenese | false | Inferred relationship | Some | 3 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Finding site | Eye structure | false | Inferred relationship | Some | 3 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Associated morphology | Kongenit hypopigmentering | false | Inferred relationship | Some | 4 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Genetic disorder of skin pigmentation (disorder) | true | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Finding site | Eye structure | true | Inferred relationship | Some | 1 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Associated morphology | Hypopigmentation | true | Inferred relationship | Some | 2 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Congenital hearing disorder | false | Inferred relationship | Some | ||
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 4 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 3 | |
Deaf blind hypopigmentation syndrome Yemenite type (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets