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1899006: Autosomal hereditary disorder (disorder)


Status: current. Date: 31-Jan 2002

Descriptions:

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


61 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal hereditary disorder Is a Hereditary disease true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive hereditary disorder Is a True Autosomal hereditary disorder Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Benign recurrent intrahepatic cholestasis Is a True Autosomal hereditary disorder Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Hyperbiliverdinaemia Is a True Autosomal hereditary disorder Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Autosomal dominant hereditary disorder Is a True Autosomal hereditary disorder Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Crigler-Najjar syndrome Is a True Autosomal hereditary disorder Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly

This concept is not in any reference sets

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