11164009: Autosomal dominant hereditary disorder (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder

Status: current. Date: 31-Jan 2002

Descriptions:

Id Description Lang Type Status Case? Module

19337016 Dominant hereditary disorder, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
195344010 Autosomal dominant hereditary disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
632967019 Autosomal dominant hereditary disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2618831016 AD - Autosomal dominant en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial porphyria cutanea tarda	Is a	True	Autosomal dominant hereditary disorder	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome	Is a	True	Autosomal dominant hereditary disorder	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
FTH1-related iron overload	Is a	True	Autosomal dominant hereditary disorder	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Arteriohepatic dysplasia	Is a	True	Autosomal dominant hereditary disorder	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly

This concept is not in any reference sets