Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3481803019 | Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481804013 | Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481805014 | Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481806010 | An extremely rare syndromic retinitis pigmentosa characterized by pigmentary retinopathy, diabetes mellitus with hyperinsulinism, acanthosis nigricans, secondary cataracts, neurogenic deafness, short stature mild hypogonadism in males and polycystic ovaries with oligomenorrhea in females. Inheritance is thought to be autosomal recessive. It can be distinguished from Alstrom syndrome by the presence of intellectual disability and the absence of renal insufficiency. There have been no further descriptions in the literature since 1993. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3481807018 | An extremely rare syndromic retinitis pigmentosa characterised by pigmentary retinopathy, diabetes mellitus with hyperinsulinism, acanthosis nigricans, secondary cataracts, neurogenic deafness, short stature mild hypogonadism in males and polycystic ovaries with oligomenorrhoea in females. Inheritance is thought to be autosomal recessive. It can be distinguished from Alstrom syndrome by the presence of intellectual disability and the absence of renal insufficiency. There have been no further descriptions in the literature since 1993. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3982621000052117 | syndrom med retinitis pigmentosa, intellektuell funktionsnedsättning, dövhet och hypogenitalism | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Hypogonadism | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | mental retardation | false | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Autosomal recessive retinitis pigmentosa | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Finding site | Ear structure | false | Inferred relationship | Some | 1 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Finding site | Gonadal endocrine structure | true | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Finding site | Retinal structure | true | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Congenital hearing disorder | false | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 5 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 6 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 6 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 7 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 7 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets