Status: current, Primitive. 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 | Case insensitive | SNOMED CT core |
3481804013 | Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3481805014 | Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome | en | Synonym | Active | Case insensitive | 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 | Case sensitive | 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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Congenital hearing disorder | false | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Finding site | Structure of auditory system | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Interprets | Hearing | true | Inferred relationship | Some | 5 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Interprets | Intellectual ability | true | Inferred relationship | Some | 6 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 6 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Interprets | Adaptation behaviour | true | Inferred relationship | Some | 7 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 7 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Hypogonadism | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Intellectual disability | false | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Autosomal recessive retinitis pigmentosa | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Finding site | Ear structure | false | Inferred relationship | Some | 1 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Finding site | Gonadal endocrine structure | true | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Associated morphology | Dystrophy | true | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Finding site | Retinal structure | true | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | Intellectual disability | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set