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1899006: Autosomal hereditary disorder (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4277013 Autosomal hereditary disorder en Synonym Active Case insensitive SNOMED CT core
4278015 Autosomal hereditary disorder, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
746648015 Autosomal hereditary disorder (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal hereditary disorder	Is a	Hereditary disease	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Insulin resistance - type A	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some
Best vitelliform macular dystrophy	Is a	False	Autosomal hereditary disorder	Inferred relationship	Some
Fundus albipunctatus	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some
Colobomatous microphthalmia, rhizomelic dysplasia syndrome	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some
Waardenburg's syndrome	Is a	False	Autosomal hereditary disorder	Inferred relationship	Some
Hartsfield syndrome	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some
Short stature due to growth hormone secretagogue receptor deficiency	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some
Genetic hyperferritinemia without iron overload	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some
Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some
Female infertility due to zona pellucida defect	Is a	True	Autosomal hereditary disorder	Inferred relationship	Some

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Reference Sets

Australian emergency department reference set

Id	Description	Lang	Type	Status	Case?	Module
4277013	Autosomal hereditary disorder	en	Synonym	Active	Case insensitive	SNOMED CT core
4278015	Autosomal hereditary disorder, NOS	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
746648015	Autosomal hereditary disorder (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core