66729008: Hemoglobin D disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D disease

\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D disease
\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D disease
\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D disease

\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D disease

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

110848014 Hemoglobin D disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

110849018 Hemoglobin D-D disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

500508012 Homozygous for Hb D en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

500509016 Haemoglobin D disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

500510014 Haemoglobin D-D disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

806374019 Hemoglobin D disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

827401000052117 hemoglobin D-sjukdom sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemoglobin D disease	Is a	Hereditary hemoglobinopathy due to globin chain mutation	true	Inferred relationship	Some
Hemoglobin D disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Hemoglobin D disease	Finding site	Erythrocyte	false	Inferred relationship	Some
Hemoglobin D disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Hemoglobin D disease	Finding site	Body system structure	false	Inferred relationship	Some
Hemoglobin D disease	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Hemoglobin D disease	Occurrence	Congenital	true	Inferred relationship	Some	1
Hemoglobin D disease	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets