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724001005: Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder)


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


0 descendants.

Expanded Value Set


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

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