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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
746648015 Autosomal hereditary disorder (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3207 descendants. Search Descendants:

Expanded Value Set

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

Clinical finding foundation reference set

Problem/Diagnosis reference set

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